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微管滑行实验中膜介导的运动动力学。

Membrane mediated motor kinetics in microtubule gliding assays.

机构信息

Department of Physics, University of California, Merced, CA, 95343, USA.

Center for Cellular and Biomolecular Machines (CCBM), University of California, Merced, CA, 95343, USA.

出版信息

Sci Rep. 2019 Jul 3;9(1):9584. doi: 10.1038/s41598-019-45847-z.

Abstract

Motor-based transport mechanisms are critical for a wide range of eukaryotic cell functions, including the transport of vesicle cargos over long distances. Our understanding of the factors that control and regulate motors when bound to a lipid substrate is however incomplete. We used microtubule gliding assays on a lipid bilayer substrate to investigate the role of membrane diffusion in kinesin-1 on/off binding kinetics and thereby transport velocity. Fluorescence imaging experiments demonstrate motor clustering on single microtubules due to membrane diffusion in the absence of ATP, followed by rapid ATP-induced dissociation during gliding. Our experimental data combined with analytical modeling show that the on/off binding kinetics of the motors are impacted by diffusion and, as a consequence, both the effective binding and unbinding rates for motors are much lower than the expected bare rates. Our results suggest that motor diffusion in the membrane can play a significant role in transport by impacting motor kinetics and can therefore function as a regulator of intracellular transport dynamics.

摘要

基于马达的运输机制对于广泛的真核细胞功能至关重要,包括囊泡货物在长距离上的运输。然而,我们对于与脂质底物结合时控制和调节马达的因素的理解并不完整。我们使用脂质双层底物上的微管滑行测定法来研究膜扩散在 kinesin-1 结合/解离动力学中的作用,从而研究运输速度。荧光成像实验表明,由于在没有 ATP 的情况下膜扩散,马达在单根微管上发生聚集,随后在滑行过程中迅速发生 ATP 诱导的解离。我们的实验数据与分析模型相结合表明,马达的结合/解离动力学受到扩散的影响,因此,马达的有效结合和解离速率都远低于预期的裸速率。我们的结果表明,膜中的马达扩散可以通过影响马达动力学在运输中发挥重要作用,因此可以作为细胞内运输动力学的调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e82d/6610617/cd3ba7e2ceff/41598_2019_45847_Fig1_HTML.jpg

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