西亚试剂优势供应上万种化学试剂产品,欢迎各位新老客户咨询、选购!

登录

¥0.00

联系方式:400-990-3999 / 邮箱:sales@xiyashiji.com

西亚试剂 —— 品质可靠,值得信赖

西亚试剂:How kinesin waits between steps

How kinesin waits between steps

Teppei Mori1, Ronald D. Vale2 & Michio Tomishige1,2

  1. Department of Applied Physics, The University of Tokyo, Tokyo 113-8656, Japan
  2. Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, California 94158, USA

Correspondence to: Ronald D. Vale2 Correspondence and requests for materials should be addressed to R.D.V. (Email: vale@cmp.ucsf.edu).

Kinesin-1 (conventional kinesin) is a dimeric motor protein that carries cellular cargoes along microtubules1, 2 by hydrolysing ATP3 and moving processively in 8-nm steps4. The mechanism of processive motility involves the hand-over-hand motion of the two motor domains ('heads')5, 6, 7, a process driven by a conformational change in the neck-linker domain of kinesin8, 9, 10, 11, 12. However, the 'waiting conformation' of kinesin between steps remains controversial13, 14, 15, 16—some models propose that kinesin adopts a one-head-bound intermediate17, 18, 19, 20, 21, whereas others suggest that both the kinesin heads are bound to adjacent tubulin subunits7, 22, 23. Addressing this question has proved challenging, in part because of a lack of tools to measure structural states of the kinesin dimer as it moves along a microtubule. Here we develop two different single-molecule fluorescence resonance energy transfer (smFRET) sensors to detect whether kinesin is bound to its microtubule track by one or two heads. Our FRET results indicate that, while moving in the presence of saturating ATP, kinesin spends most of its time bound to the microtubule with both heads. However, when nucleotide binding becomes rate-limiting at low ATP concentrations, kinesin waits for ATP in a one-head-bound state and makes brief transitions to a two-head-bound intermediate as it walks along the microtubule. On the basis of these results, we suggest a model for how transitions in the ATPase cycle position the two kinesin heads and drive their hand-over-hand motion.