Challenges and opportunities in the high-resolution cryo-EM visualization of microtubules and their binding partners

被引:17
作者
Nogales, Eva [1 ,2 ,3 ,4 ]
Kellogg, Elizabeth H. [4 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, 229 Stanley Hall, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Inst QB3, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[4] Lawrence Berkeley Natl Lab, Mol Biophys & Integrat Bioimaging, Berkeley, CA 94720 USA
关键词
NDC80 KINETOCHORE COMPLEX; 8 ANGSTROM RESOLUTION; ALPHA-BETA-TUBULIN; CRYOELECTRON MICROSCOPY; STRUCTURAL TRANSITIONS; DYNAMIC INSTABILITY; MOTOR PROTEINS; INSIGHTS; MECHANISM; LATTICE;
D O I
10.1016/j.sbi.2017.06.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As non-crystallizable polymers, microtubules have been the target of cryo-electron microscopy (cryo-EM) studies since the technique was first established. Over the years, image processing strategies have been developed that take care of the unique, pseudo-helical symmetry of the microtubule. With recent progress in data quality and data processing, cryo-EM reconstructions are now reaching resolutions that allow the generation of atomic models of microtubules and the factors that bind them. These include cellular partners that contribute to microtubule cellular functions, or small ligands that interfere with those functions in the treatment of cancer. The stage is set to generate a family portrait for all identified microtubule interacting proteins and to use cryo-EM as a drug development tool in the targeting of tubulin.
引用
收藏
页码:65 / 70
页数:6
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