Myosin motors: missing structures and hidden springs

被引:127
|
作者
Houdusse, A
Sweeney, HL
机构
[1] CNRS, Inst Curie, UMR 144, F-75248 Paris 05, France
[2] Univ Penn, Sch Med, Dept Physiol, Philadelphia, PA 19104 USA
关键词
D O I
10.1016/S0959-440X(00)00188-3
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
High-resolution structures of the motor domain of myosin II and lower resolution actin-myosin structures have led to the 'swinging lever arm' model for myosin force generation, The available kinetic data are not all easily reconciled with this model and understanding the final details of the myosin motor mechanism must await actin-myosin co-crystals. The observation that myosin can populate multiple states in the absence of actin has nonetheless led to significant insights. The currently known myosin structures correspond to defined kinetic states that bind weakly (K-d > muM) to actin, It is possible that the myosin lever arm could complete its swing before strong binding to actin and force generation - a process that would correspond, in the absence of load,to a Brownian ratchet. We further suggest that, under load, internal springs within the myosin head could decouple force generation and lever arm movement.
引用
收藏
页码:182 / 194
页数:13
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