ben-Avraham D, Tirion M M
Department of Physics, Clarkson University, Potsdam, New York 13699-5820, USA.
Biophys J. 1995 Apr;68(4):1231-45. doi: 10.1016/S0006-3495(95)80299-7.
We examine the dynamic, elastic, and mechanical consequences of the proposed atomic models of F-actin, using a normal mode analysis. This initial analysis is done in vacuo and assumes that all monomers are rigid and equivalent. Our computation proceeds from the atomic level and, relying on a single fitting parameter, reproduces various experimental results, including persistence lengths, elastic moduli, and contact energies. The computations reveal modes of motion characteristic to all polymers, such as longitudinal pressure waves, torsional waves, and bending, as well as motions unique to F-actin. Motions typical to actin include a "groove-swinging" motion of the two long-pitch helices, as well as an axial slipping motion of the two strands. We prepare snapshots of thermally activated filaments and quantify the accumulation of azimuthal angular "disorder," variations in cross-over lengths, and various other fluctuations. We find that the orientation of a small number of select residues has a surprisingly large effect on the filament flexibility and elasticity characteristics.
我们使用正常模式分析来研究所提出的F-肌动蛋白原子模型的动力学、弹性和力学后果。此初始分析是在真空中进行的,并假设所有单体都是刚性且等效的。我们的计算从原子层面开始,依靠单个拟合参数,再现了各种实验结果,包括持久长度、弹性模量和接触能。计算揭示了所有聚合物共有的运动模式,如纵向压力波、扭转波和弯曲,以及F-肌动蛋白特有的运动。肌动蛋白典型的运动包括两个长螺距螺旋的“凹槽摆动”运动,以及两条链的轴向滑动运动。我们准备了热激活细丝的快照,并量化了方位角“无序”的积累、交叉长度的变化以及各种其他波动。我们发现少数选定残基的取向对细丝的柔韧性和弹性特性有着惊人的巨大影响。