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Items: 45

1.

Microtubule end conversion mediated by motors and diffusing proteins with no intrinsic microtubule end-binding activity.

Chakraborty M, Tarasovetc EV, Zaytsev AV, Godzi M, Figueiredo AC, Ataullakhanov FI, Grishchuk EL.

Nat Commun. 2019 Apr 11;10(1):1673. doi: 10.1038/s41467-019-09411-7.

2.

The binding of Borealin to microtubules underlies a tension independent kinetochore-microtubule error correction pathway.

Trivedi P, Zaytsev AV, Godzi M, Ataullakhanov FI, Grishchuk EL, Stukenberg PT.

Nat Commun. 2019 Feb 8;10(1):682. doi: 10.1038/s41467-019-08418-4.

3.

Clot Contraction Drives the Translocation of Procoagulant Platelets to Thrombus Surface.

Nechipurenko DY, Receveur N, Yakimenko AO, Shepelyuk TO, Yakusheva AA, Kerimov RR, Obydennyy SI, Eckly A, Léon C, Gachet C, Grishchuk EL, Ataullakhanov FI, Mangin PH, Panteleev MA.

Arterioscler Thromb Vasc Biol. 2019 Jan;39(1):37-47. doi: 10.1161/ATVBAHA.118.311390.

PMID:
30580561
4.

Probing Mitotic CENP-E Kinesin with the Tethered Cargo Motion Assay and Laser Tweezers.

Gudimchuk N, Tarasovetc EV, Mustyatsa V, Drobyshev AL, Vitre B, Cleveland DW, Ataullakhanov FI, Grishchuk EL.

Biophys J. 2018 Jun 5;114(11):2640-2652. doi: 10.1016/j.bpj.2018.04.017.

5.

In vitro reconstitution of lateral to end-on conversion of kinetochore-microtubule attachments.

Chakraborty M, Tarasovetc EV, Grishchuk EL.

Methods Cell Biol. 2018;144:307-327. doi: 10.1016/bs.mcb.2018.03.018. Epub 2018 May 11.

6.

Microtubule Tip Tracking by the Spindle and Kinetochore Protein Ska1 Requires Diverse Tubulin-Interacting Surfaces.

Monda JK, Whitney IP, Tarasovetc EV, Wilson-Kubalek E, Milligan RA, Grishchuk EL, Cheeseman IM.

Curr Biol. 2017 Dec 4;27(23):3666-3675.e6. doi: 10.1016/j.cub.2017.10.018. Epub 2017 Nov 16.

7.

Biophysics of Microtubule End Coupling at the Kinetochore.

Grishchuk EL.

Prog Mol Subcell Biol. 2017;56:397-428. doi: 10.1007/978-3-319-58592-5_17. Review.

PMID:
28840247
8.

Mechanisms to Avoid and Correct Erroneous Kinetochore-Microtubule Attachments.

Lampson MA, Grishchuk EL.

Biology (Basel). 2017 Jan 5;6(1). pii: E1. doi: 10.3390/biology6010001. Review.

9.

Bistability of a coupled Aurora B kinase-phosphatase system in cell division.

Zaytsev AV, Segura-Peña D, Godzi M, Calderon A, Ballister ER, Stamatov R, Mayo AM, Peterson L, Black BE, Ataullakhanov FI, Lampson MA, Grishchuk EL.

Elife. 2016 Jan 14;5:e10644. doi: 10.7554/eLife.10644.

10.

Molecular and Mechanical Causes of Microtubule Catastrophe and Aging.

Zakharov P, Gudimchuk N, Voevodin V, Tikhonravov A, Ataullakhanov FI, Grishchuk EL.

Biophys J. 2015 Dec 15;109(12):2574-2591. doi: 10.1016/j.bpj.2015.10.048.

11.

Basic mechanism for biorientation of mitotic chromosomes is provided by the kinetochore geometry and indiscriminate turnover of kinetochore microtubules.

Zaytsev AV, Grishchuk EL.

Mol Biol Cell. 2015 Nov 5;26(22):3985-98. doi: 10.1091/mbc.E15-06-0384. Epub 2015 Sep 30.

12.

Mitosis. Microtubule detyrosination guides chromosomes during mitosis.

Barisic M, Silva e Sousa R, Tripathy SK, Magiera MM, Zaytsev AV, Pereira AL, Janke C, Grishchuk EL, Maiato H.

Science. 2015 May 15;348(6236):799-803. doi: 10.1126/science.aaa5175. Epub 2015 Apr 23.

13.

Multisite phosphorylation of the NDC80 complex gradually tunes its microtubule-binding affinity.

Zaytsev AV, Mick JE, Maslennikov E, Nikashin B, DeLuca JG, Grishchuk EL.

Mol Biol Cell. 2015 May 15;26(10):1829-44. doi: 10.1091/mbc.E14-11-1539. Epub 2015 Mar 25.

14.

Tubulin bond energies and microtubule biomechanics determined from nanoindentation in silico.

Kononova O, Kholodov Y, Theisen KE, Marx KA, Dima RI, Ataullakhanov FI, Grishchuk EL, Barsegov V.

J Am Chem Soc. 2014 Dec 10;136(49):17036-45. doi: 10.1021/ja506385p. Epub 2014 Nov 25.

15.

Accurate phosphoregulation of kinetochore-microtubule affinity requires unconstrained molecular interactions.

Zaytsev AV, Sundin LJ, DeLuca KF, Grishchuk EL, DeLuca JG.

J Cell Biol. 2014 Jul 7;206(1):45-59. doi: 10.1083/jcb.201312107. Epub 2014 Jun 30.

16.

Kinetochore-microtubule attachment throughout mitosis potentiated by the elongated stalk of the kinetochore kinesin CENP-E.

Vitre B, Gudimchuk N, Borda R, Kim Y, Heuser JE, Cleveland DW, Grishchuk EL.

Mol Biol Cell. 2014 Aug 1;25(15):2272-81. doi: 10.1091/mbc.E14-01-0698. Epub 2014 Jun 11.

17.

Preparation of segmented microtubules to study motions driven by the disassembling microtubule ends.

Volkov VA, Zaytsev AV, Grishchuk EL.

J Vis Exp. 2014 Mar 15;(85). doi: 10.3791/51150.

18.

Highly Transient Molecular Interactions Underlie the Stability of Kinetochore-Microtubule Attachment During Cell Division.

Zaytsev AV, Ataullakhanov FI, Grishchuk EL.

Cell Mol Bioeng. 2013 Dec 13;6(4). doi: 10.1007/s12195-013-0309-4.

19.

Kinetochore kinesin CENP-E is a processive bi-directional tracker of dynamic microtubule tips.

Gudimchuk N, Vitre B, Kim Y, Kiyatkin A, Cleveland DW, Ataullakhanov FI, Grishchuk EL.

Nat Cell Biol. 2013 Sep;15(9):1079-1088. doi: 10.1038/ncb2831. Epub 2013 Aug 18.

20.

A slippery walk to the microtubule-end.

Grishchuk EL.

Biophys J. 2013 Jun 4;104(11):2324-5. doi: 10.1016/j.bpj.2013.04.037. No abstract available.

21.

Long tethers provide high-force coupling of the Dam1 ring to shortening microtubules.

Volkov VA, Zaytsev AV, Gudimchuk N, Grissom PM, Gintsburg AL, Ataullakhanov FI, McIntosh JR, Grishchuk EL.

Proc Natl Acad Sci U S A. 2013 May 7;110(19):7708-13. doi: 10.1073/pnas.1305821110. Epub 2013 Apr 22.

22.

Conserved and divergent features of kinetochores and spindle microtubule ends from five species.

McIntosh JR, O'Toole E, Zhudenkov K, Morphew M, Schwartz C, Ataullakhanov FI, Grishchuk EL.

J Cell Biol. 2013 Feb 18;200(4):459-74. doi: 10.1083/jcb.201209154.

23.

The kinetochore-bound Ska1 complex tracks depolymerizing microtubules and binds to curved protofilaments.

Schmidt JC, Arthanari H, Boeszoermenyi A, Dashkevich NM, Wilson-Kubalek EM, Monnier N, Markus M, Oberer M, Milligan RA, Bathe M, Wagner G, Grishchuk EL, Cheeseman IM.

Dev Cell. 2012 Nov 13;23(5):968-80. doi: 10.1016/j.devcel.2012.09.012. Epub 2012 Oct 18. Erratum in: Dev Cell. 2012 Nov 13;23(5):1081.

24.

Tubulin depolymerization may be an ancient biological motor.

McIntosh JR, Volkov V, Ataullakhanov FI, Grishchuk EL.

J Cell Sci. 2010 Oct 15;123(Pt 20):3425-34. doi: 10.1242/jcs.067611. Review.

25.

In vitro assays to study the tracking of shortening microtubule ends and to measure associated forces.

Grishchuk EL, Ataullakhanov FI.

Methods Cell Biol. 2010;95:657-76. doi: 10.1016/S0091-679X(10)95033-4. Review.

26.
27.

Toward a comprehensive and quantitative understanding of intracellular microtubule organization.

Grishchuk EL.

Mol Syst Biol. 2009;5:251. doi: 10.1038/msb.2009.7. Epub 2009 Mar 17. No abstract available.

28.

The human kinetochore Ska1 complex facilitates microtubule depolymerization-coupled motility.

Welburn JP, Grishchuk EL, Backer CB, Wilson-Kubalek EM, Yates JR 3rd, Cheeseman IM.

Dev Cell. 2009 Mar;16(3):374-85. doi: 10.1016/j.devcel.2009.01.011.

29.

Kinesin-8 from fission yeast: a heterodimeric, plus-end-directed motor that can couple microtubule depolymerization to cargo movement.

Grissom PM, Fiedler T, Grishchuk EL, Nicastro D, West RR, McIntosh JR.

Mol Biol Cell. 2009 Feb;20(3):963-72. doi: 10.1091/mbc.E08-09-0979. Epub 2008 Nov 26.

30.

Fibrils connect microtubule tips with kinetochores: a mechanism to couple tubulin dynamics to chromosome motion.

McIntosh JR, Grishchuk EL, Morphew MK, Efremov AK, Zhudenkov K, Volkov VA, Cheeseman IM, Desai A, Mastronarde DN, Ataullakhanov FI.

Cell. 2008 Oct 17;135(2):322-33. doi: 10.1016/j.cell.2008.08.038.

31.

The Dam1 ring binds microtubules strongly enough to be a processive as well as energy-efficient coupler for chromosome motion.

Grishchuk EL, Efremov AK, Volkov VA, Spiridonov IS, Gudimchuk N, Westermann S, Drubin D, Barnes G, McIntosh JR, Ataullakhanov FI.

Proc Natl Acad Sci U S A. 2008 Oct 7;105(40):15423-8. doi: 10.1073/pnas.0807859105. Epub 2008 Sep 29. Erratum in: Proc Natl Acad Sci U S A. 2008 Dec 9;105(49):19562.

32.

Different assemblies of the DAM1 complex follow shortening microtubules by distinct mechanisms.

Grishchuk EL, Spiridonov IS, Volkov VA, Efremov A, Westermann S, Drubin D, Barnes G, Ataullakhanov FI, McIntosh JR.

Proc Natl Acad Sci U S A. 2008 May 13;105(19):6918-23. doi: 10.1073/pnas.0801811105. Epub 2008 May 6.

33.

In search of an optimal ring to couple microtubule depolymerization to processive chromosome motions.

Efremov A, Grishchuk EL, McIntosh JR, Ataullakhanov FI.

Proc Natl Acad Sci U S A. 2007 Nov 27;104(48):19017-22. Epub 2007 Nov 20.

34.

Measurement of the force developed by disassembling microtubule during calcium-induced depolymerization.

Molodtsov MI, Grishchuk EL, McIntosh JR, Ataullakhanov FI.

Dokl Biochem Biophys. 2007 Jan-Feb;412:18-21. No abstract available.

PMID:
17506346
35.

Mitotic chromosome biorientation in fission yeast is enhanced by dynein and a minus-end-directed, kinesin-like protein.

Grishchuk EL, Spiridonov IS, McIntosh JR.

Mol Biol Cell. 2007 Jun;18(6):2216-25. Epub 2007 Apr 4.

36.

Microtubule depolymerization can drive poleward chromosome motion in fission yeast.

Grishchuk EL, McIntosh JR.

EMBO J. 2006 Oct 18;25(20):4888-96. Epub 2006 Oct 12.

37.

Chromosome segregation in fission yeast with mutations in the tubulin folding cofactor D.

Fedyanina OS, Mardanov PV, Tokareva EM, McIntosh JR, Grishchuk EL.

Curr Genet. 2006 Nov;50(5):281-94. Epub 2006 Sep 27.

PMID:
17004072
38.

Force production by disassembling microtubules.

Grishchuk EL, Molodtsov MI, Ataullakhanov FI, McIntosh JR.

Nature. 2005 Nov 17;438(7066):384-8.

PMID:
16292315
39.

Force production by depolymerizing microtubules: a theoretical study.

Molodtsov MI, Grishchuk EL, Efremov AK, McIntosh JR, Ataullakhanov FI.

Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4353-8. Epub 2005 Mar 14.

40.

A molecular-mechanical model of the microtubule.

Molodtsov MI, Ermakova EA, Shnol EE, Grishchuk EL, McIntosh JR, Ataullakhanov FI.

Biophys J. 2005 May;88(5):3167-79. Epub 2005 Feb 18.

42.

Chromosome-microtubule interactions during mitosis.

McIntosh JR, Grishchuk EL, West RR.

Annu Rev Cell Dev Biol. 2002;18:193-219. Epub 2002 Apr 2. Review.

PMID:
12142285
43.

[Overexpression of the apc10+ gene in the fission yeast Schizosaccharomyces pombe can suppress temperature sensitivity of the nuc2-663 mutant,but not its sterility].

Grishchuk EL, Frolov DIu, Savchenko GV.

Mol Biol (Mosk). 2000 Sep-Oct;34(5):809-15. Russian. No abstract available.

PMID:
11033806
44.

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