Mosby, L.S., Straube, A. & Polin, M. (2023)
A general model for the motion of multivalent cargo interacting with substrates.
J. R. Soc. Interface 20: 20230510.
[Link]

Sittewelle, M. & Royle, S.J. (2023)
Passive diffusion accounts for the majority of intracellular nanovesicle transport
Life Sci Alliance 7 (1) e202302406 [Link]

Chew Y-M & Cross R.A. (2023)
Taxol acts differently on different tubulin isotypes
Comms. Biol. (6) 946 [Link]

Sittewelle, M., Ferrandiz, N., Fesenko, M. & Royle, S.J. (2023)
Genetically encoded imaging tools for investigating cell dynamics at a glance.
J. Cell Sci. 136 (7): jcs260783 [Link]

McAinsh AD, Kops GJPL. (2023)
Principles and dynamics of spindle assembly checkpoint signalling.
Nat Rev Mol Cell Biol. Mar 24. doi: 10.1038/s41580-023-00593-z. [Link]

Straube A. (2023)
The cell biology of motors.
J. Cell Sci. 136(5): jcs261056. doi: 10.1242/jcs.261056. [Link]

Arora AS, Huang HL, Singh R, Narui Y, Suchenko A, Hatano T, Heissler SM, Balasubramanian MK, Chinthalapudi K. (2023)
Structural insights into actin isoforms.
Elife. 12:e82015. doi: 10.7554/eLife.82015. [Link]

Pardal A.J. & Bowman A.J. (2022)
A specific role for importin-5 and NASP in the import and nuclear hand-off of monomeric H3.
eLife 11:e81755 [Link]

Embacher, P.A., Germanova, T.E., Roscioli, E., McAinsh, A.D. & Burroughs, N.J. (2022)
Bayesian inference of multi-point macromolecular architecture mixtures at nanometre resolution.
PLoS Comput Biol. 18(12):e1010765 [Link]

Sugawa, M., Maruyama, Y., Yamagishi, M., Cross, R.A. & Yajima, J. (2022)
Motor generated torque drives coupled yawing and orbital rotations of kinesin coated gold nanorods
Commun Biol. 5(1):1368 [Link]

Currie, C.E., Ford, E., Benham Whyte, L., Taylor, D.M., Mihalas, B.P., Erent, M., Marston, A.L., Hartshorne, G.M. & McAinsh, A.D. (2022)
The first mitotic division of human embryos is highly error prone
Nat Commun. 13(1):6755 [Link]

Chin, S.M., Hatano, T., Sivashanmugam, L., Suchenko, A., Kashina, A.S., Balasubramanian, M.K. & Jansen, S. (2022)
N-terminal acetylation and arginylation of actin determines the architecture and assembly rate of linear and branched actin networks.
J Biol Chem. 298(11):102518 [Link]

Hatano, T., Lim, T.C., Billault-Chaumartin, I., Dhar, A., Gu, Y., Massam-Wu, T., Scott, W., Adishesha, S., Chapa-Y-Lazo, B., Springall, L., Sivashanmugam, L., Mishima, M., Martin, S.G., Oliferenko, S., Palani, S. & Balasubramanian, M.K. (2022)
mNG-tagged fusion proteins and nanobodies to visualize tropomyosins in yeast and mammalian cells.
J Cell Sci. 135(18):jcs260288 [Link]

McAinsh, A.D. & Marston, A.L. (2022)
The Four Causes: The Functional Architecture of Centromeres and Kinetochores
Annu Rev Genet. doi: 10.1146/annurev-genet-072820-034559. [Link]

Castrogiovanni, C., Inchingolo, A.V., Harrison, J.U., Dudka, D., Sen, O., Burroughs, N.J., McAinsh, A.D. & Meraldi, P. (2022)
Evidence for a HURP/EB free mixed-nucleotide zone in kinetochore-microtubules
Nat Commun. 13(1):4704. doi: 10.1038/s41467-022-32421-x. [Link]

Siddiqui, N., Roth, D., Toleikis, A., Zwetsloot, A.J., Cross, R.A. & Straube, A. (2022)
Force generation of KIF1C is impaired by pathogenic mutations
Current Biology 32 [Link]

Küey, C., Sittewelle, M., Larocque, G., Hernández-González, M. & Royle, S.J. (2022)
Recruitment of clathrin to intracellular membranes is sufficient for vesicle formation
eLife, doi: 10.7554/eLife.78929 [Link]

Toh PJY, Lai JKH, Hermann A, Destaing O, Sheetz MP, Sudol M, Saunders TE. (2022)
Optogenetic control of YAP cellular localisation and function
EMBO Rep. 23(9):e54401. doi: 10.15252/embr.202154401. [Link]

Mendieta-Serrano MA, Dhar S, Ng BH, Narayanan R, Lee JJY, Ong HT, Toh PJY, Röllin A, Roy S, Saunders TE. (2022)
Slow muscles guide fast myocyte fusion to ensure robust myotome formation despite the high spatiotemporal stochasticity of fusion events
Dev Cell. S1534-5807(22)00563-9. doi: 10.1016/j.devcel.2022.08.002. [Link]

Larocque, G. & Royle, S.J. (2022)
Integrating intracellular nanovesicles into integrin trafficking pathways and beyond
Cell. Mol. Life Sci. 79: 335. doi: doi.org/10.1007/s00018-022-04371-6 [Link]

Koester, D.V., Bhat, A., Talluri, S., & Mayor S. (2022)
Reconstitution of Membrane-tethered Minimal Actin Cortices on Supported Lipid Bilayers
J Vis Exp. 12;(185). doi: 10.3791/63968. [Link]

Hatano T, Palani S, Papatziamou D, Salzer R, Souza DP, Tamarit D, Makwana M, Potter A, Haig A, Xu W, Townsend D, Rochester D, Bellini D, Hussain HMA, Ettema TJG, Lowe J, Baum B, Robinson NP, Balasubramanian M. (2022)
Asgard archaea shed light on the evolutionary origins of the eukaryotic ubiquitin-ESCRT machinery
Nat Commun.13(1):3398. doi: 10.1038/s41467-022-30656-2 [Link]

Ferrandiz, N., Downie, L., Starling, G.P. and Royle, S.J. (2022)
Endomembranes promote chromosome missegregation by ensheathing misaligned chromosomes
J Cell Biol 2022 Jun 6;221(6). pii:jcb.202203021. doi: 10.1083/jcb.202203021 [Link]

Alvarez, Y. & Smutny, M. (2022)
Emerging Role of Mechanical Forces in Cell Fate Acquisition
Front Cell Dev Biol. 10:864522. doi: 10.3389/fcell.2022.864522 [Link]

Harrison JU, Sen O, McAinsh AD, Burroughs NJ. (2022)
Kinetochore tracking in 3D from lattice light sheet imaging data with KiT.
Bioinformatics. 2022 May 17:btac330. doi: 10.1093/bioinformatics/btac330. [Link]

Wontakal SN, Britto M, Zhang H, Han Y, Gao C, Tannenbaum S, Durham BH, Lee MT, An X, Mishima M. (2022)
RACGAP1 variants in a sporadic case of CDA III implicate the dysfunction of centralspindlin as the basis of the disease.
Blood. 2022 Mar 3;139(9):1413-1418. doi: 10.1182/blood.2021012334. [Link]

Mahabaleshwar H, Asharani PV, Loo TY, Koh SY, Pitman MR, Kwok S, Ma J, Hu B, Lin F, Li Lok X, Pitson SM, Saunders TE, Carney TJ. (2022)
Slit-Robo signalling establishes a Sphingosine-1-phosphate gradient to polarise fin mesenchyme
EMBO Rep. 23(8):e54464. doi: 10.15252/embr.202154464. [Link]

Lai JKH, Toh PJY, Cognart HA, Chouhan G, Saunders TE. (2022)
DNA-damage induced cell death in yap1;wwtr1 mutant epidermal basal cells
Elife. 11:e72302. doi: 10.7554/eLife.72302. [Link]

Karkali K, Tiwari P, Singh A, Tlili S, Jorba I, Navajas D, Muñoz JJ, Saunders TE, Martin-Blanco E. (2022)
Condensation of the Drosophila nerve cord is oscillatory and depends on coordinated mechanical interactions
Dev Cell. 57(7):867-882.e5. doi: 10.1016/j.devcel.2022.03.007. [Link]

de-Carvalho J, Tlili S, Hufnagel L, Saunders TE, Telley IA. (2022)
Aster repulsion drives short-ranged ordering in the Drosophila syncytial blastoderm
Development. 149(2):dev199997. doi: 10.1242/dev.199997. [Link]

Germanova TE, Roscioli E, Harrison JU, McAinsh AD, Burroughs NJ. (2021)
Subcellular Euclidean distance measurements with multicolor fluorescence localization imaging in cultured cells.
STAR Protoc. 2021 Nov 15;2(4):100774. doi: 10.1016/j.xpro.2021.100774. [Link]

Blackley DG, Cooper JH, Pokorska P, Ratheesh A. (2021)
Mechanics of developmental migration.
Semin Cell Dev Biol. 2021 Dec;120:66-74. doi: 10.1016/j.semcdb.2021.07.002. [Link]

Inman A, Smutny M. (2021)
Feeling the force: Multiscale force sensing and transduction at the cell-cell interface.
Semin Cell Dev Biol. 2021 Dec;120:53-65. doi: 10.1016/j.semcdb.2021.06.006. [Link]

Sen O, Harrison JU, Burroughs NJ, McAinsh AD. (2021)
Kinetochore life histories reveal an Aurora-B-dependent error correction mechanism in anaphase.
Dev Cell. 2021 Nov 22;56(22):3082-3099.e5. doi: 10.1016/j.devcel.2021.10.007. [Link]

Baker, A.N.; Richards, S.-J.; Pandey, S.; Guy, C.; Ahmad, A.; Hasan, M.; Biggs, C.; Georgiou, P.; Zwetsloot, A.; Straube, A.; Dedola, S.; Field, R.; Grammatopoulos, D.; Anderson, N.; Walker, M.; and Gibson, M. (2021)
A Glycan-based Flow-Through Device for the Detection of SARS-COV-2.
ACS Sensors 2021, doi: 10.1021/acssensors.1c01470
[Link]

Smith, S.M., Larocque, G., Wood, K.M., Morris, K.L., Roseman, A.M., Sessions, R.B., Royle, S.J. & Smith, C.J. (2021)
Multi-modal adaptor-clathrin contacts drive coated vesicle assembly.
EMBO J e108795.
doi: 10.15252/embj.2021108795 [Link]

Yin Ho Vong, Lavanya Sivashanmugam, Rebecca Leech, Andreas Zaucker, Alex Jones, Karuna Sampath (2021)
The RNA-binding protein Igf2bp3 is critical for embryonic and germline development in zebrafish .
PLoS Genet 17(7): e1009667.
doi: 10.1371/journal.pgen.1009667 [Link]

Larocque, G., Moore, D.J., Sittewelle, M., Kuey, C., Hetmanski, J.H.R, La-Borde, P.J., Wilson, B.J., Clarke, N.I., Caswell, P.T. and Royle, S.J (2021)
Intracellular nanovesicles mediate α5β1 integrin trafficking during cell migration.
J Cell Biol 220 (10): e202009028.
doi: 10.1083/jcb.202009028 [Link]

Palani S, Ghosh S, Ivorra-Molla E, Clarke S, Suchenko A, Balasubramanian MK, Koester DV. (2021)
Calponin-homology domain mediated bending of membrane associated actin filaments.
eLife 10:e61078.
doi: 10.7554/eLife.61078 [Link]

Gharanei S, Fishwick K, Peter Durairaj R, Jin T, Siamantouras E, Liu K-K, Straube A, Lucas ES, Weston CJ, Rantakari P, Salmi M, Jalkanen S, Brosens JJ and Tan BK (2021)
Vascular Adhesion Protein-1 Determines the Cellular Properties of Endometrial Pericytes.
Front. Cell Dev. Biol. 8:621016.
doi: 10.3389/fcell.2020.621016 [Link]

Malek, S., Köster, D.V. (2021)
The Role of Cell Adhesion and Cytoskeleton Dynamics in the Pathogenesis of the Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders
Frontiers in Cell and Developmental Biology
doi: 10.3389/fcell.2021.649082 [Link]

M. del Mar Aguilo-Ferretjans, R. Bosch, R. J. Puxty, M. Latva, V. Zadjelovic, A. Chhun, D. Sousoni, M. Polin, D. J. Scanlan, and J. A. Christie-Oleza (2021)
Pili allow dominant marine cyanobacteria to avoid sinking and evade predation.
Nature Communications 12, 1857
doi: https://doi.org/10.1038/s41467-021-22152-w [Link]

Maruyama Y, Sugawa M, Yamaguchi S, Davies T, Osaki T, Kobayashi T, Yamagishi M, Takeuchi S, Mishima M, Yajima J. M. del Mar Aguilo-Ferretjans, R. Bosch, R. J. Puxty, M. Latva, V. Zadjelovic, A. Chhun, D. Sousoni, M. Polin, D. J. Scanlan, and J. A. Christie-Oleza (2021)
CYK4 relaxes the bias in the off-axis motion by MKLP1 kinesin-6.
Commun Biol. 4:180. doi: 10.1038/s42003-021-01704-2
[Link]

I. Lopez-Grobas, M. Polin*, and M. Asally* (2021)
Swarming bacteria undergo localized dynamic phase transition to form stress-induced biofilms.
(* Joint last authors). eLife 10, e62632 doi: 10.7554/eLife.62632 [Link]

H. L. Devereux, C. R. Twomey, M. S. Turner and S. Thutupalli (2021)
Whirligig beetles as corralled active Brownian particles
J. R. Soc. Interface, 18, 20210114 doi: 10.1098/rsif.2021.0114 [Link]

A. E. B. T. King and M.S.Turner (2021)
Non-local interactions in collective motion,
R. Soc. Open Sci. 8, 201536 [Link]

Ryan*, E.L., Shelford*, J., Massam-Wu, T., Bayliss, R. & Royle, S.J. (2020)
Defining endogenous TACC3–chTOG–clathrin–GTSE1 interactions at the mitotic spindle using induced relocalization
Journal of Cell Science 134(3):jcs255794 [Link]

Algirdas Toleikis, Nicholas J. Carter & Robert A. Cross (2020)
Backstepping mechanism of kinesin
Biophysical Journal 119, 1984-1994
doi.org/10.1016/j.bpj.2020.09.034
[Link]

Roscioli E, Germanova TE, Smith CA, Embacher PA, Erent M, Thompson AI, Burroughs NJ, McAinsh AD. (2020)
Ensemble-Level Organization of Human Kinetochores and Evidence for Distinct Tension and Attachment Sensors
Cell Reports 31(4):107535
doi.10.1016/j.celrep.2020.107535
[Link]

Yean Ming Chew & Robert A. Cross (2020)
Molecular Motors: Kif14's disordered dongle
Current Biology 30 R988-R990
DOI: 10.1016/j.cub.2020.06.095
[Link]

Piermarco Fonda, Sami C Al-Izzi, Luca Giomi, Matthew S Turner (2020)
Measuring Gaussian Rigidity Using Curved Substrates.
Phys Rev Lett 125(18):188002. doi: 10.1103/PhysRevLett.125.188002. [Link]

Alexander N. Baker, Sarah-Jane Richards, Collette S. Guy, Thomas R. Congdon, Muhammad Hasan, Alexander J. Zwetsloot, Angelo Gallo, Józef R. Lewandowski, Phillip J. Stansfeld, Anne Straube, Marc Walker, Simona Chessa, Giulia Pergolizzi, Simone Dedola, Robert A. Field, and Matthew I. Gibson (2020)
The SARS-COV-2 Spike Protein Binds Sialic Acids and Enables Rapid Detection in a Lateral Flow Point of Care Diagnostic Device.
ACS Central Science 6 (11): 2046–2052 doi: 10.1021/acscentsci.0c00855
[Link]

Al-Izzi, S.C. Sens, P., Turner, M.S. and Komura, S. (2020)
Dynamics of passive and active membrane tubes
Soft Matter 2020 doi: 10.1039/d0sm01290d
[Link]

Francesca Bottanelli, Bruno Cadot, Felix Campelo, Scott Curran, Patricia M. Davidson, Gautam Dey, Ishier Raote, Anne Straube and Matthew P. Swaffer (2020)
Science during lockdown – from virtual seminars to sustainable online communities
Journal of Cell Science 2020 133: jcs249607
[Link]

Nida Siddiqui and Anne Straube (2020)
The Kinesin-3 Family: Long-Distance Transporters
in: The Kinesin Superfamily Handbook: Transporter, Creator, Destroyer, ed. Claire T. Friel, CRC Press, 2020
[Link to Book] [Open Access Chapter]

Auckland, P., Roscioli, E., Coker, H.L.E., McAinsh, A.D. (2020)
CENP-F stabilizes kinetochore-microtubule attachments and limits dynein stripping of corona cargoes.
Journal of Cell Biology. Vol. 219 No. 5 e201905018 [Open]

Mosby, L.S., Hundt, N., Young, G., Fineberg, A., Polin, M., Mayor, S., Kukura, P. & Köster, D.V. (2020)
Myosin II filament dynamics in actin networks revealed with interferometric scattering microscopy.
Biophysical Journal. 2020.02.025. doi: 10.1016/j.bpj.2020.02.025. [Open]

Palani S., Köster D., Balasubramanian M., (2020)
Phosphoregulation of tropomyosin-actin interaction revealed using a genetic code expansion strategy.
Wellcome Open Research. doi: 10.12688/wellcomeopenres.16082.1. [Open]

Mosby L., Polin M., Köster D. (2020)
A Python based automated tracking routine for myosin II filaments.
Journal of Physics D: Applied Physics. doi: 10.1088/1361-6463/ab87bf. [Open]

Das, A.*, Bhat, A.*, Sknepnek, R., Köster, D., Mayor, S., Rao, M (2020)
Stratification relieves constraints from steric hindrance in the generation of compact actomyosin asters at the membrane cortex.
Science Advances. doi: 10.1126/sciadv.aay6093. [Open]

Koester, D.V. (2020)
Pulling of Tethers from the Cell Plasma Membrane Using Optical Tweezers.
Methods Mol Biol. 2169:167-174. doi: 10.1007/978-1-0716-0732-9_15. [Link]

Chapa-Y-Lazo, B., Hamanaka, M., Wray, A., Balasubramanian, M.K., & Mishima, M. (2020)
Polar relaxation by dynein-mediated removal of cortical myosin II.
J Cell Biol. 219(8). pii: e201903080. doi: 10.1083/jcb.201903080. [Link]

Rushworth, L.K., Hewit, K., Munnings-Tomes, S., Somani, S., James, D., Shanks, E., Dufes, C., Straube, A., Patel, R., & Leung, H.Y. (2020)
Repurposing screen identifies mebendazole as a clinical candidate to synergise with docetaxel for prostate cancer treatment.
Br J Cancer. 122(4):517-527. doi: 10.1038/s41416-019-0681-5. [Open]

Larocque, G., La-Borde, P.J., Clarke, N.I., Carter, N.J. & Royle, S.J. (2020)
Tumor Protein D54 defines a new class of intracellular transport vesicles.
The Journal of Cell Biology. 219: e 201812044. doi: 10.1083/jcb.201812044. [Open]

Jeanneret, R., Pushkin, D.O. & Polin, M. (2019)
Confinement Enhances the Diversity of Microbial Flow Fields..
Phys Rev Lett. 123(24):248102. doi: 10.1103/PhysRevLett.123.248102. [Open]

Küey, C., Larocque, G., Clarke, N.I & Royle, S.J. (2019)
Unintended inhibition of protein function using GFP nanobodies in human cells.
Journal of Cell Science. 132: jcs234955. doi: 10.1242/jcs.234955. [Open]

Capalbo, L., Bassi, Z.I., Geymonat, M., Todesca, S., Copoiu, L., Enright, A.J., Callaini, G., Riparbelli, M.G., Yu, L., Choudhary, J.S., Ferrero, E., Wheatley, S., Douglas, M.E., Mishima, M. & D'Avino, P.P. (2019)
The midbody interactome reveals unexpected roles for PP1 phosphatases in cytokinesis.
Nat Commun. 10(1):4513. doi: 10.1038/s41467-019-12507-9. [Open]

Adib R, Montgomery JM, Atherton J, O'Regan L, Richards MW, Straatman KR, Roth D, Straube A, Bayliss R, Moores CA, Fry AM. (2019)
Mitotic phosphorylation by NEK6 and NEK7 reduces the microtubule affinity of EML4 to promote chromosome congression.
Sci Signal. 12(594):eaaw2939. doi: 10.1126/scisignal.aaw2939. [Link]

Shah, P., Chaumet, A., Royle, S.J. & Bard, F.A. (2019)
The NAE Pathway: Autobahn to the Nucleus for Cell Surface Receptors.
Cells, 33: 119-20. doi: 10.3390/cells8080915. [Open]

Clare Garcin and Anne Straube (2019)
Microtubules in cell migration
Essays in Biochemistry 63(5): 509-520.
doi: 10.1042/EBC20190016 [Link]

N. Siddiqui*, A.J. Zwetsloot*, A. Bachmann, D. Roth, H. Hussain, J. Brandt, I. Kaverina & A. Straube (2019)
PTPN21 and Hook3 relieve KIF1C autoinhibition and activate intracellular transport
Nature Communications, Volume 10, Article number: 2693 doi: 10.1038/s41467-019-10644-9 [Link]

O. Von Loeffelholz, A. Peña, D.R. Drummond, R.A. Cross, C.A. Moores (2019)
4.5 Å Cryo-EM Structure of Yeast Kinesin-5-Microtubule Complex Reveals a Distinct Binding Footprint and Mechanism of Drug Resistance
J. Mol. Biol. doi: 10.1016/j.jmb.2019.01.011 [Link]

Bazarova, A., Nieduszynski, C.A., Akerman, I. and Burroughs, N.J. (2019)
Bayesian inference of origin firing time distributions, origin interference and licencing probabilities from Next Generation Sequencing data
Nucleic Acids Research. 2019, 47:2229–2243 [Link]

Cheffings, T.H. Burroughs, N.J. and Balasubramanian, M.K. (2019)
Actin turnover ensures uniform tension distribution during cytokinetic actomyosin ring contraction
Mol. Biol. Cell. 2019, 30(8):933-941. [Link]

Stanfield, Z., Lai, P.F., Lei, K., Johnson, M.R., Blanks, A.M., Romero, R., Chance, M.R., Mesiano, S. and Koyutürk, M. (2019)
Myometrial Transcriptional Signatures of Human Parturition
Front. Genet. [Link]

Syed, J., Palani, S., Clarke, S.T., Asad, Z., Bottrill, A.R., Jones, A.M.E., Sampath, K. and Balasubramanian, M.K. (2019)
Expanding the Zebrafish Genetic Code through Site-Specific Introduction of Azido-lysine, Bicyclononyne-lysine, and Diazirine-lysine
Int. J. Mol. Sci. [Link]

Zaucker, A, Kumari, P and K Sampath (2019)
Zebrafish embryogenesis - A framework to study regulatory RNA elements in development and disease
Developmental Biology [Link]

Dewulf, M., Köster, D., Sinha, B., Viaris de Lesegno, C., Chambon, V., Bigot, A., Bensalah, M., Negroni, E., Tardif, N., Podkalicka, J., Johannes, L., Nassoy, P., Butler-Browne, G., Lamaze, C. and Blouin, C.M. (2019)
Dystrophy-associated caveolin-3 mutations reveal that caveolae couple IL6/STAT3 signaling with mechanosensing in human muscle cells.
Nature Communications, 10 (1) 1974 [Link]

Ditlev, J.A., Vega, A.R., Köster, D.V., Su, X., Tani, T., Lakoduk, A.M., Vale, R.D., Mayor, S., Jaqaman, K., and Rosen, M.K. (2019)
A composition-dependent molecular clutch between T cell signaling condensates and actin
eLife 8:e42695 [Link]

Cross, R.A. (2019)
Microtubule lattice plasticity
Current Opinion in Cell Biology, doi: 10.1242/jcs.219550 [Link]

Slator P.J. & Burroughs, N.J. (2018)
A Hidden Markov Model for Detecting Confinement in Single-Particle Tracking Trajectories
Biophys J. 2018 Nov 6; 115(9): 1741–1754 [Link]

Lutton EJ, Lammers WJEP, James S, van den Berg HA, Blanks AM (2018)
Identification of uterine pacemaker regions at the myometrial-placental interface in the rat
J Physiol. 2018 Jul;596(14):2841-2852. doi: 10.1113/JP275688 [Link]

Liu, Y., Claydon, R., Polin, M. and Brumley, D.R. (2018)
Transitions in synchronization states of model cilia through basal-connection coupling
Journal of The Royal Society Interface, doi: 10.1098/rsif.2018.0450 [Link]

Roth, D., Fitton, B.P., Chmel, N., Wasiluk, N. and Straube, A. (2018)
Spatial positioning of EB family proteins at microtubule tips involves distinct nucleotide-dependent binding properties
Journal of Cell Science 132:jcs219550
doi: 10.1242/jcs.219550 [Link]

Zwetsloot, A.J., Tut, G. and Straube, A. (2018)
Measuring microtubule dynamics
Essays in Biochemistry 62(6):725-735, doi: 10.1042/EBC20180035 [Link]

Currie CE, Mora-Santos M, Smith CA, McAinsh AD and Millar JBA. (2018)
Bub1 is not essential for the checkpoint response to unattached kinetochores in diploid human cells.
Current Biology 28, 929-930. [Link]

John C Meadows, Liam J Messin, Anton Kamnev, Theresa C Lancaster, Mohan K Balasubramanian, Robert A Cross, Jonathan BA Millar (2018)
Opposing kinesin complexes queue at plus tips to ensure microtubule catastrophe at cell ends
EMBO reports (2018) e46196 doi:10.15252/embr.201846196 [Link]

Wood, L.A. & Royle, S.J. (2018)
Imaging "Hot-Wired" Clathrin-Mediated Endocytosis.
Methods Mol Biol. 1847: 83-94. doi: 10.1007/978-1-4939-8719-1_7. [Link]

Clarke, N.I. & Royle, S.J. (2018)
Correlating light microscopy with serial block face scanning electron microscopy to study mitotic spindle architecture.
Methods Cell Biol. 145: 29-43. doi: 10.1016/bs.mcb.2018.03.010. [Link]

Clarke, N.I. & Royle, S.J. (2018)
FerriTag is a new genetically-encoded inducible tag for correlative light-electron microscopy.
Nat Commun. 9: 2604. doi: 10.1038/s41467-018-04993-0. [Link]

Baniukiewicz, P., Collier, S. & Bretschneider, T. (2018)
QuimP: analyzing transmembrane signalling in highly deformable cells.
Bioinformatics. bty169. [Link]

Dudka, D., Noatynska, A., Smith, C.A, Liaudet, N., McAinsh, A.D. & Meraldi, P. (2018)
Complete microtubule–kinetochore occupancy favours the segregation of merotelic attachments.
Nat Commun. 9: 2042. [Link]

McHugh, T., Drechsler, H., McAinsh, A.D., Carter, N.J. & Cross R.A. (2018)
Kif15 functions as an active mechanical ratchet.
Mol Biol Cell. mbcE18030151. doi: 10.1091/mbc.E18-03-0151. [Link]

Al-Izzi, S.C., Rowlands, G., Sens, P & Turner, M.S. (2018)
Hydro-osmotic Instabilities in Active Membrane Tubes.
Phys Rev Lett. 120(13):138102. doi: 10.1103/PhysRevLett.120.138102. [Link]

Peet, D.R., Burroughs, N.J. & Cross, R.A. (2018)
Kinesin expands and stabilizes the GDP-microtubule lattice.
Nat Nanotechnol doi: 10.1038/s41565-018-0084-4 [Link]

Hatano, T., Alioto, S., Roscioli, E., Palani, S., Clarke, S.T., Kamnev, A., Hernandez-Fernaud, J.R., Sivashanmugam, L., Chapa, Y.L.B., Jones, A.M.E., Robinson, R.C., Sampath, K., Mishima, M., McAinsh, A.D., Goode, B.L. & Balasubramanian, M.K. (2018)
Rapid production of pure recombinant actin isoforms in Pichia pastoris.
J Cell Sci doi: 10.1242/jcs.213827 [Link]

Burgess, S.G., Mukherjee, M., Sabir, S., Joseph, N., Gutierrez-Caballero, C., Richards, M.W., Huguenin-Dezot, N., Chin, J.W., Kennedy, E.J., Pfuhl, M., Royle, S.J., Gergely, F. & Bayliss, R. (2018)
Mitotic spindle association of TACC3 requires Aurora-A-dependent stabilization of a cryptic alpha-helix.
EMBO J doi:10.15252/embj.201797902 [Link]

Rhys, A.D., Monteiro, P., Smith, C., Vaghela, M., Arnandis, T., Kato, T., Leitinger, B., Sahai, E., McAinsh, A., Charras, G. & Godinho, S.A. (2018)
Loss of E-cadherin provides tolerance to centrosome amplification in epithelial cancer cells.
J Cell Biol doi: 10.1083/jcb.201704102 [Link]

Palani, S., Srinivasan, R., Zambon, P., Kamnev, A., Gayathri, P. & Balasubramanian, M.K. (2018)
Steric hindrance in the upper 50 kDa domain of the motor Myo2p leads to cytokinesis defects in fission yeast.
J Cell Sci doi:10.1242/jcs.205625 [Link]

Mishima, M. (2017)
Preparation of centralspindlin as an active heterotetramer of kinesin and GAP subunits for in vitro structural and functional assays
Methods Cell Biol. 2017;137:371-385. doi: 10.1016/bs.mcb.2016.04.005 [Link]

Rhys, A.D., Monteiro, P., Smith, C. Vaghela, M., Arnandis, T., Kato, T., Leitinger, B., Sahai, E., McAinsh, A., Charras, G. and Godinho, S.A. (2017) Loss of E-cadherin provides tolerance to centrosome amplification in epithelial cancer cells
Journal of Cell Biology [Link]

Ottilie von Loeffelholz, Neil A. Venables, Douglas R. Drummond, Miho Katsuki, Robert A. Cross & Carolyn A. Moores (2017)
Nucleotide– and Mal3-dependent changes in fission yeast microtubules suggest a structural plasticity view of dynamics
Nature Communications, 8: 2110 [Open]

Meadows, J.C and Millar, J.B.A. (2017)
Some assembly required: Redefining the mitotic checkpoint
Molecular & Cellular Oncology, 4(6):e1314238
[Link]

Zaucker, A., Nagorska, A., Kumari, P., Hecker, N., Wang, Y., Huang, S., Cooper, L., Sivashanmugam, L., VijayKumar, S., Brosens, J., Gorodkin, J. and Sampath, K. (2017)
Translational co-regulation of a ligand and inhibitor by a conserved RNA element Nucleic Acids Research, gkx938 [Link]

Wood, L.A., Larocque, G., Clarke, N.I., Sarkar, S. and Royle, S.J. (2017)
New tools for “hot-wiring” clathrin-mediated endocytosis with temporal and spatial precision
Journal of Cell Biology, 216: 4351-65; DOI: 10.1083/jcb.201702188
[Link]

Sarkar, S., Ryan, E.L. and Royle, S.J. (2017)
FGFR3–TACC3 cancer gene fusions cause mitotic defects by removal of endogenous TACC3 from the mitotic spindle
Open Biology, 7: 170080; DOI: 10.1098/rsob.170080
[Open]

Siddiqui, N. and Straube, A. (2017)
Intracellular cargo transport by kinesin-3 motors
Biochemistry (Moscow), Vol. 82, No. 7, pp. 803–815
Russian version: Biokhimiya, 2017, Vol. 82, No. 7, pp. 1047–1062
[open access article]

Collier, S., Paschke, P., Kay, R.R. and Bretschneider, T. (2017)
Image based modeling of bleb site selection
Scientific Reports, 7: 6692 doi: 10.1038/s41598-017-06875-9
[Open]

Chew, T.G., Huang, J., Palani, S., Sommese, R., Kamnev, A., Hatano, T., Gu, Y., Oliferenko, S., Sivaramakrishnan, S. and Balasubramanian, M.K. (2017)
Actin turnover maintains actin filament homeostasis during cytokinetic ring contraction
Journal of Cell Biology doi: 10.1083/jcb.201701104
[Open]

Nixon*, F.M., Honnor*, T.R., Clarke, N.I., Starling, G.P., Beckett, A.J., Johansen, A.M., Brettschneider, J.A., Prior, I.A. and Royle, S.J. (2017)
Microtubule organization within mitotic spindles revealed by serial block face scanning electron microscopy and image analysis
Journal of Cell Science, 130: 1845-55. doi: 10.1242/jcs.203877
[Link]

Auckland, P., Clarke, N.I., Royle, S.J. and McAinsh, A.D. (2017)
Congressing kinetochores progressively load Ska complexes to prevent force-dependent detachment
Journal of Cell Biology. 216: 1623-39. doi: 10.1083/jcb.201607096.
[Link]

Lutton, E.J., Lammers, W.J., James, S., van den Berg, H.A., Blanks, A.M. (2017)
A computational method for three-dimensional reconstruction of the microarchitecture of myometrial smooth muscle from histological sections
PLoS One. 12, e0173404 doi: 10.1371/journal.pone.0173404.
[Link]

Palani, S., Chew, T.G., Ramanujam, S., Kamnev, A., Harne, S., Chapa-Y-Lazo, B., Hogg, R., Sevugan, M., Mishra, M., Gayathri, P., and Balasubramanian, M.K. (2017)
Motor Activity Dependent and Independent Functions of Myosin II Contribute to Actomyosin Ring Assembly and Contraction in Schizosaccharomyces pombe
Current Biology. doi: 10.1016/j.cub.2017.01.028.
[Link]

Meadows, J.C., Lancaster, T.C., Buttrick, G.J., Sochaj, A.M., Messin, L.J., Mora-Santos, M.D., Hardwick, K.G. and Millar, J.B.A. (2017)
Identification of a Sgo2-Dependent but Mad2-Independent Pathway Controlling Anaphase Onset in Fission Yeast
Cell Reports. 18(6):1422-1433. doi: 10.1016/j.celrep.2017.01.032.
[Link]

Zambon, P., Palani, S., Kamnev, A. and Balasubramanian, M.K. (2017)
Myo2p is the major motor involved in actomyosin ring contraction in fission yeast
Current Biology. 27(3):R99-R100. doi: 10.1016/j.cub.2016.12.024.
[Link]

Mishima, M. (2016)
Centralspindlin in Rappaport's cleavage signaling
Semin Cell Dev Biol. 2016 May;53:45-56. doi: 10.1016/j.semcdb.2016.03.006. Epub 2016 Mar 7. Review. [Link]

Mora-Santos MD, Hervas-Aguilar A, Sewart K, Lancaster TC, Meadows JC, Millar JB (2016)
Bub3-Bub1 Binding to Spc7/KNL1 Toggles the Spindle Checkpoint Switch by Licensing the Interaction of Bub1 with Mad1-Mad2
Curr Biol. 2016 Oct 10;26(19):2642-2650. doi: 10.1016/j.cub.2016.07.040. PMID: 27618268
[Link]

Mishan Britto, Adeline Goulet, Syeda Rizvi, Ottilie von Loeffelholz, Carolyn A. Moores, and Robert A. Cross (2016)
Schizosaccharomyces pombe kinesin-5 switches direction using a steric blocking mechanism
PNAS DOI: 10.1073/pnas.1611581113
[Open]

Junqi Huang, Ting Gang Chew, Ying Gu, Saravanan Palani, Anton Kamnev, Douglas S. Martin, Nicholas J. Carter, Robert A. Cross, Snezhana Oliferenko and Mohan K Balasubramanian (2016)
Curvature-induced expulsion of actomyosin bundles during cytokinetic ring contraction
eLife 2016;10.7554/eLife.21383
[Open]

Chris A. Smith, Andrew D. McAinsh and Nigel J. Burroughs (2016)
Human kinetochores are swivel joints that mediate microtubule attachments
eLife 10.7554/eLife.16159
[Open]

Thomas H. Cheffings, Nigel J. Burroughs and Mohan K. Balasubramanian correspondence (2016)
Actomyosin Ring Formation and Tension Generation in Eukaryotic Cytokinesis
Curr Biol 26: R719-R737
[Review]

Ulrike Theisen and Anne Straube (2016)
Microtubules Regulate Cell Migration and Neuronal Pathfinding
in: The Microtubule Cytoskeleton, Jens Lüders (ed), pages 151-189 DOI: 10.1007/978-3-7091-1903-7_6
[Link]

Hervas-Aguilar A, Millar JB.
Mph1/MPS1 checks in at the kinetochore
Cell Cycle. 2016 May 18;15(10):1313-4. doi: 10.1080/15384101.2016.1159888. PMID: 27105354
[Link]

Robert A. Cross (2016)
Mechanochemistry of the kinesin-1 ATPase
Biopolymers DOI: 10.1002/bip.22862
[Open]

Hauke Drechsler and Andrew D. McAinsh (2016)
Kinesin-12 motors cooperate to suppress microtubule catastrophes and drive the formation of parallel microtubule bundles
Proc Natl Acad Sci U S A. Mar 11
[Open Access]

Jonathan W. Armond, Elina Vladimirou, Andrew D. McAinsh, and Nigel J. Burroughs (2016)
KiT: A MATLAB package for kinetochore tracking
Bioinformatics First published online: February 15
[Open Access]

Frauke Hussmann, Douglas R. Drummond, Daniel Peet, Douglas S. Martin & Robert A. Cross (2016)
Alp7/TACC-Alp14/TOG generates long-lived, fast-growing MTs by an unconventional mechanism
Nature Scientific Reports DOI: 10.1038/srep20653
[Open Access]

Joanna Andrecka, Jaime Ortega Arroyo, Katie Lewis, Robert A. Cross, and Philipp Kukura (2016)
Label-free Imaging of Microtubules with Sub-nm Precision Using Interferometric Scattering Microscopy
Biophysical Journal 110 214-217
[Link]

Davies, T., Kodera, N., Kaminski Schierle, G. S., Rees, E., Erdelyi, M., Kaminski, C. F., Ando, T., Mishima, M. (2015)
CYK4 promotes antiparallel microtubule bundling by optimizing MKLP1 neck conformation
PLoS Biol. 2015 Apr 13;13(4):e1002121. doi: 10.1371/journal.pbio.1002121 [Link]

Lee, K.-Y., Esmaeili, B., Zealley, B., Mishima, M. (2015)
Direct interaction between centralspindlin and PRC1 reinforces mechanical resilience of the central spindle
Nat Commun. 2015 Jun 19;6:7290. doi: 10.1038/ncomms8290 [Link]

Cross, R.A. (2015)
Mechanisms of action of Eg5 inhibitors
in Kinesins and Cancer ed. Frank Kozielski Springer, 2015 ISBN 978-94-017-9732-0 (ebook)
[pdf]

Patel J, Tan SL, Hartshorne GM, McAinsh AD. (2015)
Unique geometry of sister kinetochores in human oocytes during meiosis I may explain maternal age-associated increases in chromosomal abnormalities.
Biol Open. Dec 30. pii: bio.016394. doi: 10.1242/bio.016394. [Epub ahead of print]
[Open access]

Silio V, **McAinsh AD, **Millar JB. (2015)
KNL1-Bubs and RZZ Provide Two Separable Pathways for Checkpoint Activation at Human Kinetochores.
Developmental Cell. Dec 7;35(5):600-13.
[link]

Armond JW, Harry EF, McAinsh AD, Burroughs NJ. (2015)
Inferring the Forces Controlling Metaphase Kinetochore Oscillations by Reverse Engineering System Dynamics.
PLoS Computational Biology Nov 30;11(11):e1004607.
[Open access]

**Burroughs, N.J., Harry, E.F. and **McAinsh, A.D. (2015)
Super-resolution kinetochore tracking reveals the mechanisms of human sister kinetochore directional switching
eLife 2015;10.7554/eLife.09500
[link]

Straube, A. (2015)
Microtubules and Microtubule-Associated Proteins (MAPs).
Encyclopedia of Cell Biology, Volume 2: Organizational Cell Biology, 2016, Pages 539-547
[link] [request pdf]

Auckland, P. and McAinsh, A.D. (2015)
Building an integrated model of chromosome congression.
Journal of Cell Science, 128: 3363-74
[link]

Nixon, F.M., Gutiérrez-Caballero, C., Hood, F.E., Booth, D.G., Prior, I.A. & Royle, S.J. (2015)
The mesh is a network of microtubule connectors that stabilizes individual kinetochore fibers of the mitotic spindle.
eLife, 4: e07635. doi: 10.7554/eLife.07635
[link] [press] [blog]

Lee, K.Y., Esmaeili, B., Zealley, B. & Mishima, M. (2015)
Direct interaction between centralspindlin and PRC1 reinforces mechanical resilience of the central spindle.
Nature Communications, 6: 7290. doi: 10.1038/ncomms8290
[link]

Quach, H.N., Tao, S., Vrljicak, P., Joshi, A., Ruan, H., Sukumaran, R., Varshney, G.K., LaFave, M.C., Ds Screen Team, Burgess, S.M., Winkler, C., Emelyanov, A., Parinov, S., & Sampath, K. (2014)
A Multifunctional Mutagenesis System for Analysis of Gene Function in Zebrafish.
G3 (Bethesda), 5: 1283-99.
[link]

Lobo, D.P. ,Wemyss, A.M., Smith, D.J., Straube, A., Betteridge, K.B., Salmon, A.H.J., Foster, R.R., Elhegni, H.E., Satchell, S.C., Little, H.A., Pacheco-Gomez, R., Simmons, M.J., Hicks, M.R., Bates, D.O., Rodger, A., Dafforn, T.R., & Arkill, K.P. (2015)
Direct detection and measurement of wall shear stress using a filamentous bio-nanoparticle.
Nano Research, doi: 10.1007/s12274-015-0831-x [link]

Nahorski, M.S., Al-Gazali, L., Hertecant, J., Owen, D.J., Borner, G.H.H., Chen, Y., Benn, C.L., Carvalho, O.P., Shaikh, S.S., Phelan, A., Robinson, M.S., Royle, S.J. & Woods, C.G. (2015)
A novel disorder reveals clathrin heavy chain-22 is essential for human pain and touch development.
Brain, doi: 10.1093/brain/awv149
[link]

O'Regan, L., Sampson, J., Richards, M.W., Knebel, A., Roth, D., Hood, F.E., Straube, A., Royle, S.J., Bayliss, R. & Fry, A.M. (2015)
Hsp72 is targeted to the mitotic spindle by Nek6 to promote K-fiber assembly and mitotic progression.
The Journal of Cell Biology, 209: 349-358. doi:10.1083/jcb.201409151
[link]

Davies, T., Kodera, N., Kaminski Schierle, G.S., Rees, E., Erdelyi, M., Kaminski, C.F., Ando, T. & Mishima, M. (2015)
CYK4 Promotes Antiparallel Microtubule Bundling by Optimizing MKLP1 Neck Conformation.
PLoS Biology, 13: e1002121. doi: 10.1371/journal.pbio.1002121
[link]

Meadows, J.C. & Millar, J.B. (2015)
Sharpening the anaphase switch.
Biochemical Society Transactions, 43: 19-22.
[link]

Armond J.W.*, Vladimirou E.*, Erent M., McAinsh A.D.** & Burroughs N.J.** (2015)
Probing microtubule polymerisation state at single kinetochores during metaphase chromosome motion.
Journal of Cell Science, 128: 1991-2001. doi: 10.1242/jcs.168682
[Open Access PDF]

Mogessie, B., Roth, D., Rahil, Z. and Straube, A. (2015)
A novel isoform of MAP4 organises the paraxial microtubule array required for muscle cell differentiation
eLife, 4: e05697. doi:10.7554/eLife.05697.
[link] | [PDF]

Wood, L.A. & Royle, S.J. (2015)
Zero Tolerance: Amphipathic Helices in Endocytosis
Developmental Cell, 33: 119-20.
[link]

Richards, M.W., O'Regan, L., Roth, D., Montgomery, J.M., Straube, A., Fry, A.M. and Bayliss, R. (2015)
Microtubule association of EML proteins and the EML4-ALK variant 3 oncoprotein require an N-terminal trimerization domain
Biochemical Journal, 467: 529-536. doi:10.1042/BJ20150039
[link]

Gutiérrez-Caballero, C., Burgess, S.G., Bayliss, R. & Royle, S.J. (2015)
TACC3–ch-TOG track the growing tips of microtubules independently of clathrin and Aurora-A phosphorylation
Biology Open, 4: 170-9.
[OA] [preprint]

Bachmann, A. and Straube, A. (2015)
Kinesins in cell migration
Biochem Soc Trans, 43(1): 79-83.
[PDF] | [pubmed]

Royle, S.J. (2015)
Super-duper resolution imaging of mitotic microtubules
Nature Reviews Molecular Cell Biology, 16: 67.
[link]

*Bancroft, J., *Auckland, P., Samora, C.P. and McAinsh A.D. (2015)
Chromosome congression is promoted by CENP-Q- and CENP-E-dependent pathways
Journal of Cell Science, 128, 171-184. doi:10.1242/jcs.163659
[Open Access PDF]

Srinivasan, R. & Balasubramanian, M.K.(2014)
Bacteria spring a surprise.
eLife, 3: e03435.
[link]

Tao, E.Y., Calvert, M. & Balasubramanian, M.K.(2014)
Rewiring Mid1p-independent medial division in fission yeast
Current Biology, 24: 2181-8.
[link]

McAinsh A.D. (2014)
How Kinetochores CCAN resist force
Developmental cell 30 (6), 637-638
[link]

Efimova, N., Grimaldi, A., Bachmann, A., Frye, K., Zhu, X., Feoktistov, A., Straube, A. and Kaverina, I. (2014)
Podosome-regulating kinesin KIF1C translocates to the cell periphery in a CLASP-dependent manner.
Journal of Cell Science 127: 5179-5188. doi:10.1242/jcs.149633
[link]

Messin, L.J. & Millar, J.B. (2014)
Role and regulation of kinesin-8 motors through the cell cycle.
Systems and Synthetic Biology, 8: 205-13.
[link]

Grimaldi, A.D., Maki, T., Fitton, B.P., Roth, D., Yampolsky, D., Davidson, M.W., Svitkina, T., Straube, A., Hayashi, I. and Kaverina, I. (2014)
CLASPs are required for proper microtubule localization of end-binding proteins.
Developmental Cell, 30, 343-352.
[link]

López-Murcia, F.J., Royle, S.J. & Llobet, A. (2014)
Presynaptic clathrin levels are a limiting factor for synaptic transmission
J Neurosci 34: 8618-8629.
[link]

Willox, A.K., Sahraoui, Y.M.E. & Royle, S.J. (2014)
Non-specificity of Pitstop 2 in clathrin-mediated endocytosis.
Biology Open 3: 326-31. doi: 10.1242/bio.20147955 bioRxiv doi:10.1101/002675
[link] [preprint]

Cross RA and McAinsh AD (2014)
Prime movers: the mechanochemistry of mitotic kinesins.
Nature Reviews Molecular Cell Biology 15:257-271
[link]

Drechsler, H., McHugh, T., Singleton, M.R., Carter, N.J. and McAinsh, A.D. (2014)
The kinesin-12 Kif15 is a processive track-switching tetramer
eLife 3: e01724; PMID: 24668168
[pdf] [press release] [lens] [lay summary]

Vazquez-Novelle M. D., Sansregret, L., Dick, A., Smith, C. A., McAinsh, A. D., Gerlich, D. W. and Petronczki, M. (2014)
Cdk1 Inactivation Terminates Mitotic Checkpoint Surveillance and Stabilizes Kinetochore Attachments in Anaphase
Current Biology 24: 1-8 doi.org/10.1016/j.cub.2014.01.034
[link]

Kaur, S., Fielding, A.B., Gassner, G., Carter, N. J. & Royle, S.J. (2014)
An unmet actin requirement explains the mitotic inhibition of clathrin-mediated endocytosis
eLife 3: e00829 doi: 10.7554/eLife.00829
[pdf] [html] [lens]

Katsuki, M., Drummond, D.R. & Cross, R.A. (2014)
Ectopic A-lattice seams destabilise microtubules
Nature Communications, 5: 3094 doi: 10.1038/ncomms4094
[open]

Wolman, A.J.M., Sanchez-Cano, C., Carstairs, H.M.J., Cross, R.A. & Turberfield, A.J. (2014)
Transport and self-organization across different length scales powered by motor proteins and programmed by DNA
Nature Nanotechnology, 9:44-47 doi: 10.1038/nnano.2013.230
[link]

Vladimirou, E.*, Mchedlishvili, N.*, Gasic, I.*, Armond, J.W., Samora, C.P., Meraldi, P**. and McAinsh, A.D.** (2013)
Nonautonomous movement of chromosomes in mitosis.
Developmental Cell, 27: 60-71
[link]

Jefferyes, S.D.R., Epstein, D.B.A., Straube, A., Rajpoot, N.M. (2013)
A novel framework for exploratory analysis of highly variable morphology of migrating epithelial cells.
Conf Proc IEEE Eng Med Biol Soc. 2013 Jul;2013:3463-3466, doi:10.1109/EMBC.2013.6610287
[link] [pubmed abstract]

Royle, S.J. (2013)
Protein adaptation: mitotic functions for membrane trafficking proteins.
Nature Rev. Mol. Cell Biol. 14: 592-9. doi:10.1038/nrm3641
[link]

Hood, F.E., Williams, S.J., Burgess, S.G., Richards, M.W., Roth, D., Straube, A., Pfuhl, M., Bayliss, R. & Royle, S.J. (2013)
Coordination of adjacent domains mediates TACC3–ch-TOG–clathrin assembly and mitotic spindle binding.
J. Cell Biol. 202:463-78
[link]

Earnshaw WC, Allshire RC, Black BE, Bloom K, Brinkley BR, Brown W, Cheeseman IM, Choo KH, Copenhaver GP, Deluca JG, Desai A, Diekmann S, Erhardt S, Fitzgerald-Hayes M, Foltz D, Fukagawa T, Gassmann R, Gerlich DW, Glover DM, Gorbsky GJ, Harrison SC, Heun P, Hirota T, Jansen LE, Karpen G, Kops GJ, Lampson MA, Lens SM, Losada A, Luger K, Maiato H, Maddox PS, Margolis RL, Masumoto H, McAinsh AD, Mellone BG, Meraldi P, Musacchio A, Oegema K, O'Neill RJ, Salmon ED, Scott KC, Straight AF, Stukenberg PT, Sullivan BA, Sullivan KF, Sunkel CE, Swedlow JR, Walczak CE, Warburton PE, Westermann S, Willard HF, Wordeman L, Yanagida M, Yen TJ, Yoda K, Cleveland DW. (2013)
Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant.
Chromosome Research 21:101-106
[pubmed abstract]

Mora-Santos, M. & Millar, J.B. (2013)
Checkpoint proteins come under scrutiny.
eLife, 2: e01494.
[link]

Cheeseman, L.P., Harry, E.F., McAinsh, A.D., Prior, I.A. & Royle, S.J. (2013)
Specific removal of TACC3-ch-TOG-clathrin at metaphase deregulates kinetochore fiber tension.
J. Cell Sci., 126: 2102-13
[link to pdf] [pubmed abstract]

Hawkins T.L., Sept D., Mogessie B., Straube A. and Ross J.L. (2013)
Mechanical Properties of Doubly Stabilized Microtubule Filaments.
Biophysical Journal 104: 1517-1528
[link to pdf] [pubmed abstract][request pdf]

Theisen U, Straube E, and Straube A. (2012)
Directional Persistence of Migrating Cells Requires Kif1C-Mediated Stabilization of Trailing Adhesions.
Developmental Cell 23:1153-1166
[link to pdf] [pubmed abstract][request pdf]

Drechsler & McAinsh AD (2012)
Exotic mitotic mechanisms.
Open Biology. December 5
[link to pdf] [pubmed abstract][request pdf]

Eskat A, Deng W, Hofmeister A, Rudolphi S, Emmerth S, Hellwig D, Ulbricht T, Doring V, Bancroft JM, McAinsh AD, Cardoso MC, Meraldi P, Hoischen C, Leonhardt H, Diekmann S. (2012)
Step-Wise Assembly, Maturation and Dynamic Behavior of the Human CENP-P/O/R/Q/U Kinetochore Sub-Complex.
PLOS ONE. 7:e44717
[link to pdf] [pubmed abstract][request pdf]

Joseph, N., Hutterer, A., Poser, I., Mishima, M. (2012)
ARF6 GTPase protects the post-mitotic midbody from 14-3-3-mediated disintegration
EMBO J. 31:2604-14
[link to pdf] [pubmed abstract][request pdf]

Erent, M., Drummond, D.R., Cross R.A (2012)
S. pombe kinesins-8 promote both nucleation and catastrophe of microtubules
PLoS ONE 7, e30738 - e30738
[link to pdf]

Kaseda, K., McAinsh, A.D. & Cross, R.A. (2012)
Dual pathway spindle assembly increases both the speed and the fidelity of mitosis
Biology Open, Nov 2. doi: 10.1242/​bio.2011012
[link to pdf] [Biology Open website]

McAinsh, A.D. & Straube, A. (2011)
Spindle Centricity
Cell Cycle, Advance Online Publication December 1
[link to pdf][request pdf]

Hellwig, D., Emmerth, S., Ulbricht, t., Doring, V., Hoischen, C., Martin, R., Samora. C, McAinsh, A.D., Carroll, C.W., Straight, A.F., Meraldi, P., and Diekmann, S. (2011)
Dynamics of CENP‐N kinetochore binding during the cell cycle
J Cell Sci , Advance Online Publication November 18
[link to pdf] [pubmed abstract]

Grant, B.J., Gheorghe, D., Zheng,W., Alonso, M., Huber, G., Dlugosz,M., McCammon, J.A. & Cross, R.A. (2011)
Electrostatically biased binding of kinesin to microtubules
PLOS Biology 9(11) e1001207. Epub 2011 Nov 29
[link to pdf] [pubmed abstract]

McAinsh, A.D. & Meraldi, P.. (2011)
The CCAN complex: Linking centromere specification to control of kinetochore-microtubule dynamics
Seminars in Cell and Developmental Biology, Oct 19. [Epub ahead of print]
[link to pdf] [pubmed abstract]

Cross, R.A., McAinsh, A.D. & Straube A. (2011)
Mechanochemical Cell Biology
Seminars in Cell and Developmental Biology, Oct 7. [Epub ahead of print]
[link to pdf] [pubmed abstract]

Drummond, D.R. (2011)
Regulation of microtubule dynamics by kinesins
Seminars in Cell and Developmental Biology, Oct 5. [Epub ahead of print]
[link to pdf] [pubmed abstract]

Kaverina, I. & Straube A. (2011)
Regulation of cell migration by dynamic microtubules
Seminars in Cell and Developmental Biology, 22 968-974
[pubmed abstract] [link to pdf] [link to free pdf]

Samora, C.P.*, Mogessie, B.*, Conway, L., Ross, J.L., Straube, A.** & McAinsh A.D.** (2011)
MAP4 and CLASP1 operate as a safety mechanism to maintain a stable spindle position in mitosis.
Nature Cell Biology, 131040-1050
[link to pdf] [pubmed abstract]

Straube A. (2011)
How to measure microtubule dynamics?
Methods in Molecular Biology, 777 1-14
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Samora, C.P & McAinsh A.D. (2011)
Photoactivatable-GFP-α-Tubulin as a Tool to Study Microtubule Plus-End Turnover in Living Human Cells.
Methods in Molecular Biology, 777 223-33
[link to pdf] [pubmed abstract]

Drummond D.R., Kain S., Newcombe A., Hoey C., Katsuki M., Cross R.A. (2011)
Purification of Tubulin from the Fission Yeast Schizosaccharomyces pombe.
Methods in Molecular Biology, 777 29-55
[link to pdf] [pubmed abstract]

Katsuki M., Muto E., Cross R.A. (2011)
Preparation of dual-color polarity-marked fluorescent microtubule seeds.
Methods in Molecular Biology, 777 117-26
[link to pdf] [pubmed abstract]

Vladimirou E., Harry, E., Burroughs N. & McAinsh A.D. (2011)
Springs, clutches and motors: driving forward kinetochore mechanism by modelling
Chromosome Biology, 19 409-21
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*equal contribution **corresponding authors

Cross RA (2010)
Kinesin-14: the roots of reversal
BMC Biology 12 8:107
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Amaro AC, Samora CP, Holtackers R, Wang E, Kingston I, Alonso M, Lampson L, McAinsh AD** and Meraldi P** (2010)
Molecular control of kinetochore-microtubule dynamics and chromosome oscillation
Nature Cell Biology, 12 319-329
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Jaqaman K*, King E*, Amaro AC*, Winter JR*, Dorn JF, Elliott, HL, Mchedlishvili N, McClelland SE, Porter IM, Posch M, Toso A, Danuser G**, McAinsh AD**, Meraldi P**, Swedlow JR** (2010)
Kinetochore alignment within the metaphase plate is regulated by centromere stiffness and microtubule depolymerases
Journal of Cell Biology, 188 665-79
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*equal contribution **corresponding authors