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Publications

2020

  • Benarroch, JM. and Asally, M. (2020) The Microbiologist’s Guide to Membrane Potential Dynamics. Trends in Microbiology, DOI:10.1016/j.tim.2019.12.008.

2019

  • Charmet, J.; Rodrigues, R.; Yildirim, E.; Challa, P.K.; Roberts, B.; Dallmann, R.; Whulanza, Y. (2019) Low Cost Microfabrication Tool Box. Preprints, 2019120371.
  • Clark, R., Usselmann L., Brown MR., Goeppert AU., Corrigan A. (2019) A flexible high content imaging assay for profiling macrophage efferocytosis. J Immunol Methods, DOI: 10.1016/j.jim.2019.112636.
  • Kyle L. Morris, Joseph R. Jones, Mary Halebian, Shenping Wu, Michael Baker, Jean-Paul Armache, Amaurys Avila Ibarra, Richard B. Sessions, Alexander D. Cameron, Yifan Cheng and Corinne J. Smith (2019) Cryo-EM of multiple cage architectures reveals a universal mode of clathrin self-assembly Nature Structural & Molecular Biology, DOI: 10.1038/s41594-019-0292-0.
  • Christopher Stubbs, Thomas Congdon, Jessica Davis, Daniel Lester, Sarah-Jane Richards, and Matthew I. Gibson (2019) High-Throughput Tertiary Amine Deoxygenated Photopolymerizations for Synthesizing Polymer Libraries. Macromolecules, DOI: 10.1021/acs.macromol.9b01714.
  • Jonathan S. Fenn, Ridvan Nepravishta, Collette S. Guy, James Harrison, Jesus Angulo, Alexander D. Cameron, Elizabeth Fullam (2019) Structural Basis of Glyceroplosphodiester Recognition by the Myobacterium tuberculosis Substrate-Binding Protein UgpB. American Chemical Society DOI: 10.1021/acschembio.9b00204
  • Dunford, J.R., Lutton E.J., Atia J.,, Blanks A. M., van den Berg H.A., (2019) Computational physiology of uterine smooth muscle. Science Progress, DOI: 10.1177/0036850419850431.
  • Zwetsloot, A. J., Tut, G., & Straube, A. (2018) Measuring microtubule dynamics. Essays in Biochemistry, 62(6), 725-735, DOI: 10.1042/EBC20180035.
  • Emanuele Roscioli, Tvetselina Germanova, Chris A. Smith, Peter A. Embacher, Muriel Erent, Amelia I. Thompson, Nigel J. Burroughs, Andrew D. McAinsh (2019) Ensemble-level organization of human kinetochores and evidence for distinct tension and attachment sensors bioRxiv 685248, DOI: 10.1101/685248.
  • Nida Siddiqui, Alexander James Zwetsloot, Alice Bachmann, Daniel Roth, Hamdi Hussain, Jonathan Brandt, Irina Kaverina & Anne Straube (2019) PTPN21 and Hook3 relieve KIF1C autoinhibition and activate intracellular transport. Nature Communications, DOI: 10.1038/s41467-019-10644-9.

  • Alonso J. Pardal, Filipe Fernandes-Duarte and Andrew J. Bowman (2019) The histone chaperoning pathway: from ribosome to nucleosome. Essays in Biochemistry, DOI: 10.1042/EBC20180055.
  • Sarah A. Richardson, Thomas M. Rawlings, Joanne Muter, Marc Walker, Jan J. Brosens, Neil R. Cameron, Ahmed M. Eissa (2019) Covalent Attachment of Fibronectin onto Emulsion-Templated Porous Polymer Scaffolds Enhances Human Endometrial Stromal Cell Adhesion, Infiltration, and Function. Macromolecular Bioscience, DOI: 10.1002/mabi.201800351.
  • Arnaud Kengmo Tchoupa, Rebekah A Jones, Agnes Kuroki, Mohammad Tauqeer Alam, Sebastien Perrier, Yin Chen and Meera Unnikrishnan (2019) The type VII secretion system protects Staphylococcus aureus against antimicrobial host fatty acids. BioRXiv, DOI: 10.1101/572172v1.

  • Vlisidou, I., Hapeshi, A., Healey, J.R.J., Smart, K.,Yang G., Waterfield, N.R., (2019) Photorhabdus Virulence Cassettes: extracellular multi-protein needle complexes for delivery of small protein effectors into host cells. BioRXiv, DOI: 10.1101/549964v1.
  • Teja Sirec, Jonatan M. Benarroch, Pauline Buffard, Jordi Garcia-Ojalvo, Munehiro Asally (2019) Electrical polarization enables integrative quality control during bacterial differentiation into spores. iScience, DOI: 10.1016/j.isci.2019.05.044.
  • Alexia Hapeshi, Jonatan M. Benarroch, David J. Clarke and Nicholas R. Waterfield (2019) Iso-propyl stilbene: a life cycle signal? Microbiology, 165: 516-526, DOI: 10.1099/mic.0.000790.

2018

  • Zwetsloot, A. J., Tut, G., Straube, A., (2018) Measuring microtubule dynamics, Essays in Biochemistry, DOI: 10.1042/EBC20180035.
  • Pesenti, M. E., Prumbaum, D., Auckland, P., Smith, C. M., Faesen, A. C., Petrovic, A., Erent, M., Maffini, S., Pentakota, S., Weir, J. R., Lin, Y. C., Raunser, S., McAinsh, A. D., Musacchio, A. Reconstitution of a 26-Subunit Human Kinetochore Reveals Cooperative Microtubule Binding by CENP-OPQUR and NDC80. Molecular Cell, 71: 923-939.e10, DOI: 10.1016/j.molcel.2018.07.038.
  • Bridge, L.J., Mead, J., Frattini, E., Winfield, I., Ladds, G. (2018) Modelling and simulation of biased agonism dynamics at a G protein-coupled receptor. J Theor Biol. 442:44-65, DOI: 10.1016/j.jtbi.2018.01.010.
  • eadows, J.C., Messin, L.J., Kamnev, A., Lancaster, T.C, Balasubramanian, M.K., Cross, R.A., Millar, J.B.A. (2018). Opposing kinesin complexes queue at plus tips to ensure microtubule catastrophe at cell ends. EMBO Reports, 19:e46196, DOI: 10.15252/embr.201846196.

2017

  • Halebian, M., Morris, K., Smith, C., (2017) Structure and Assembly of Clathrin Cages. Subcell Biochem, 83:551-567, DOI: 10.1007/978-3-319-46503-6_20.
  • Smith, S.M., Baker, M., Halebian, M. and Smith, C.J. (2017) Weak Molecular Interactions in Clathrin-Mediated Endocytosis. Front Mol Biosci, DOI: 10.3389/fmolb.2017.00072.
  • Wood, L., Larocque, G., Clarke, N.I., Sarkar, S., Royle, S.J. (2017) New tools for “hot-wiring” clathrin-mediated endocytosis with temporal and spatial precision. Journal of Cell Biology, DOI: 10.1083/jcb.201702188.
  • Auckland, P., Clarke, N.I., Royle, S.J., McAinsh, A.D. (2017) Congressing kinetochores progressively load Ska complexes to prevent force-dependent detachment. Journal of Cell Biology, DOI: 10.1083/jcb.201607096.
  • Meadows, J.C., Lancaster, T.C., Buttrick, G.J., Sochaj, A.M., Mora Santos, M., Messin, L., Mora Santos, M.d.M., Hardwick, K.G. and Millar, J.B. (2017), Identification of a Sgo2-dependent but Mad2-independent pathway controlling anaphase onset in fission yeast. Cell Reports, 18:1422-1433. DOI: 10.1016/j.celrep.2017.01.032.

2016

  • de Wolf E., van de Wiel J., Cook J., Dale N. (2016) Altered CO2 sensitivity of connexin26 mutant hemichannels in vitro. Physiol Rep, 4:e13038, DOI: 10.14814/phy2.13038.
  • Weston, C., Winfield, I., Harris, M., Hodgson, R., Shah, A., Dowell, S.J., Mobarec, J.C., Woodcock, D.A., Reynolds, C.A., Poyner, D.R., Watkins, H.A., Ladds, G. (2016) Receptor activity modifying protein-directed G protein signaling specificity for the calcitonin gene-related peptide family of receptors. Journal of Biological Chemistry, DOI: 10.1074/jbc.M116.751362.
  • Wood, L.A., Clarke, N.I., Sarkar, S. & Royle, S.J. (2016) Hot-wiring clathrin-mediated endocytosis in human cells. BioRxiv, DOI: 10.1101/061986.
  • Knight, A., Hemmings, J.L., Winfield, I., Leuenberger, M., Frattini, E., Frenguelli, B.G., Dowell, S.J., Lochner, M., Ladds, G. (2016) Discovery of Novel Adenosine Receptor Agonists that Exhibit Subtype Selectivity. Journal of Medicinal Chemisty. 59, 947-964, DOI: 10.1021/acs.jmedchem.5b01402.

2015

  • Auckland, P. and McAinsh, A.D. (2015) Building an integrated model of chromosome congression. Journal of Cell Science, 128, 3363-74.
  • Wood, L.A. and Royle, S.J. (2015) Zero Tolerance: Amphipathic Helices in Endocytosis Developmental Cell, 33, 119-20.
  • *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.

Pre-2014

  • Messin, L.J., Millar, J.B. (2014) Role and regulation of kinesin-8 motors through the cell cycle. Systems Synthetic Biology 8, 205-13.
  • Shepperd, L.A., Meadows, J.C., Sochaj, A.M., Lancaster, T.C., Zou, J., Buttrick, G.J., Rappsilber, J., Hardwick, K.G., Millar, J.B. (2012) Phosphodependent recruitment of Bub1 and Bub3 to Spc7/KNL1 by Mph1 kinase maintains the spindle checkpoint. Current Biology 22, 891-9
  • Meadows, J.C., Shepperd, L.A., Vanoosthuyse, V., Lancaster, T.C., Sochaj, A.M., Buttrick, G.J., Hardwick, K.G., Millar, J.B. (2011) Spindle checkpoint silencing requires association of PP1 to both Spc7 and kinesin-8 motors. Developmental Cell. 20, 739-50.