Department of Physics, University of California, Merced, CA, 95343, USA.
Center for Cellular and Biomolecular Machines (CCBM), University of California, Merced, CA, 95343, USA.
Sci Rep. 2019 Jul 3;9(1):9584. doi: 10.1038/s41598-019-45847-z.
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.
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。