Uemura Sotaro, Higuchi Hideo, Olivares Adrian O, De La Cruz Enrique M, Ishiwata Shin'ichi
Department of Physics, School of Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555, Japan.
Nat Struct Mol Biol. 2004 Sep;11(9):877-83. doi: 10.1038/nsmb806. Epub 2004 Aug 1.
Myosin V is a double-headed processive molecular motor that moves along an actin filament by taking 36-nm steps. Using optical trapping nanometry with high spatiotemporal resolution, we discovered that there are two possible pathways for the 36-nm steps, one with 12- and 24-nm substeps, in this order, and the other without substeps. Based on the analyses of effects of ATP, ADP and 2,3-butanedione 2-monoxime (a reagent shown here to slow ADP release from actomyosin V) on the dwell time and the occurrence frequency of the main and the intermediate states, we propose that the 12-nm substep occurs after ATP binding to the bound trailing head and the 24-nm substep results from a mechanical step following the isomerization of an actomyosin-ADP state on the bound leading head. When the isomerization precedes the 12-nm substep, the 36-nm step occurs without substeps.
肌球蛋白V是一种双头持续性分子马达,它沿着肌动蛋白丝以36纳米的步长移动。利用具有高时空分辨率的光镊纳米技术,我们发现36纳米步长存在两种可能的途径,一种依次有12纳米和24纳米的子步长,另一种没有子步长。基于对ATP、ADP和2,3-丁二酮单肟(一种在此显示可减缓ADP从肌动球蛋白V释放的试剂)对停留时间以及主要和中间状态出现频率的影响分析,我们提出12纳米子步长出现在ATP与结合的拖尾头部结合之后,而24纳米子步长是由结合的领头头部上的肌动球蛋白-ADP状态异构化后的机械步长导致的。当异构化先于12纳米子步长时,36纳米步长则无分子步长地发生。