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对 dynein 环的角测量揭示了一个依赖于柔性茎的步进机制。

Angular measurements of the dynein ring reveal a stepping mechanism dependent on a flexible stalk.

机构信息

Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, PA 19104.

Pennsylvania Muscle Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.

出版信息

Proc Natl Acad Sci U S A. 2017 Jun 6;114(23):E4564-E4573. doi: 10.1073/pnas.1620149114. Epub 2017 May 22.

Abstract

The force-generating mechanism of dynein differs from the force-generating mechanisms of other cytoskeletal motors. To examine the structural dynamics of dynein's stepping mechanism in real time, we used polarized total internal reflection fluorescence microscopy with nanometer accuracy localization to track the orientation and position of single motors. By measuring the polarized emission of individual quantum nanorods coupled to the dynein ring, we determined the angular position of the ring and found that it rotates relative to the microtubule (MT) while walking. Surprisingly, the observed rotations were small, averaging only 8.3°, and were only weakly correlated with steps. Measurements at two independent labeling positions on opposite sides of the ring showed similar small rotations. Our results are inconsistent with a classic power-stroke mechanism, and instead support a flexible stalk model in which interhead strain rotates the rings through bending and hinging of the stalk. Mechanical compliances of the stalk and hinge determined based on a 3.3-μs molecular dynamics simulation account for the degree of ring rotation observed experimentally. Together, these observations demonstrate that the stepping mechanism of dynein is fundamentally different from the stepping mechanisms of other well-studied MT motors, because it is characterized by constant small-scale fluctuations of a large but flexible structure fully consistent with the variable stepping pattern observed as dynein moves along the MT.

摘要

动力蛋白的产生力的机制与其他细胞骨架马达的产生力的机制不同。为了实时检查动力蛋白步进机制的结构动力学,我们使用具有纳米精度定位的偏振全内反射荧光显微镜来跟踪单个马达的方向和位置。通过测量与动力蛋白环偶联的单个量子纳米棒的偏振发射,我们确定了环的角位置,发现它在行走时相对于微管(MT)旋转。令人惊讶的是,观察到的旋转很小,平均只有 8.3°,并且与步幅相关性很弱。在环的两侧两个独立标记位置的测量结果显示出类似的小旋转。我们的结果与经典的力冲程机制不一致,而是支持一种柔性茎干模型,其中头部之间的应变通过茎干的弯曲和铰链旋转环。基于 3.3μs 分子动力学模拟确定的茎干和铰链的机械顺应性解释了实验中观察到的环旋转程度。这些观察结果共同表明,动力蛋白的步进机制与其他经过充分研究的 MT 马达的步进机制根本不同,因为它的特征是大但灵活的结构的恒定小尺度波动,与沿着 MT 移动的动力蛋白的可变步进模式完全一致。

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