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本文引用的文献

1
Nonprocessive motor dynamics at the microtubule membrane tube interface.微管膜管界面处非进行性马达动力学。
Biophys J. 2010 Jan 6;98(1):93-100. doi: 10.1016/j.bpj.2009.09.058.
2
Dynamic kinesin-1 clustering on microtubules due to mutually attractive interactions.由于相互吸引作用,动力蛋白-1在微管上动态聚集。
Phys Biol. 2008 Nov 24;5(4):046004. doi: 10.1088/1478-3975/5/4/046004.
3
Bidirectional membrane tube dynamics driven by nonprocessive motors.由非持续性马达驱动的双向膜管动力学。
Proc Natl Acad Sci U S A. 2008 Jun 10;105(23):7993-7. doi: 10.1073/pnas.0709677105. Epub 2008 Mar 10.
4
Coordination of Kinesin motors pulling on fluid membranes.驱动蛋白马达拉动流体膜的协同作用。
Biophys J. 2008 Jun;94(12):5009-17. doi: 10.1529/biophysj.107.118554. Epub 2008 Feb 29.
5
Critical fluctuations of tense fluid membrane tubules.紧张的流体细胞膜微管的临界涨落
Phys Rev Lett. 2007 Jan 5;98(1):018103. doi: 10.1103/PhysRevLett.98.018103.
6
Kinesin moving through the spotlight: single-motor fluorescence microscopy with submillisecond time resolution.驱动蛋白穿越聚光灯:具有亚毫秒时间分辨率的单分子荧光显微镜技术
Biophys J. 2007 Apr 1;92(7):2536-45. doi: 10.1529/biophysj.106.093575. Epub 2007 Jan 19.
7
Cooperative cargo transport by several molecular motors.几种分子马达协同进行的货物运输。
Proc Natl Acad Sci U S A. 2005 Nov 29;102(48):17284-9. doi: 10.1073/pnas.0507363102. Epub 2005 Nov 15.
8
Kinesin and dynein move a peroxisome in vivo: a tug-of-war or coordinated movement?驱动蛋白和动力蛋白在体内移动过氧化物酶体:拔河比赛还是协同运动?
Science. 2005 Jun 3;308(5727):1469-72. doi: 10.1126/science.1108408. Epub 2005 Apr 7.
9
Force barriers for membrane tube formation.膜管形成的力屏障。
Phys Rev Lett. 2005 Feb 18;94(6):068101. doi: 10.1103/PhysRevLett.94.068101. Epub 2005 Feb 16.
10
Synthesis and preliminary physical applications of a rhodamin-biotin phosphatidylethanolamine, an easy attainable lipid double probe.
Chem Phys Lipids. 2005 Feb;133(2):215-23. doi: 10.1016/j.chemphyslip.2004.10.005. Epub 2004 Dec 8.

在固定膜管中回收驱动蛋白。

Kinesin recycling in stationary membrane tubes.

机构信息

Physics of Life Processes, Leiden Institute of Physics, Leiden University, Leiden, The Netherlands.

出版信息

Biophys J. 2010 Sep 22;99(6):1835-41. doi: 10.1016/j.bpj.2010.06.071.

DOI:10.1016/j.bpj.2010.06.071
PMID:20858428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2940996/
Abstract

Collections of motors dynamically organize to extract membrane tubes. These tubes grow but often pause or change direction as they traverse an underlying microtubule (MT) network. In vitro, membrane tubes also stall: they stop growing in length despite a large group of motors available at the tip to pull them forward. In these stationary membrane tubes in vitro, we find that clusters of processive kinesin motors form and reach the tip of the tube at regular time intervals. The average times between cluster arrivals depends on the time over which motors depart from the tip, suggesting that motors are recycled toward the tip. Numerical simulations of the motor dynamics in the membrane tube and on the MTs show that the presence of cooperative binding between motors quantitatively accounts for the clustering observed experimentally. Cooperative binding along the length of the MT and a nucleation point at a distance behind the tip define the recycling period. Based on comparison of the numerical results and experimental data, we estimate a cooperative binding probability and concentration regime where the recycling phenomenon occurs.

摘要

马达的集合体动态组织起来以提取膜管。这些管在生长,但在穿过下面的微管(MT)网络时经常暂停或改变方向。在体外,膜管也会停滞:尽管尖端有大量的马达可以拉动它们向前,但它们的长度不再增长。在体外这些静止的膜管中,我们发现,连续运动的驱动蛋白马达簇形成并以固定的时间间隔到达管的尖端。簇到达的平均时间间隔取决于马达从尖端离开的时间,这表明马达被回收至尖端。对膜管和 MT 上的马达动力学的数值模拟表明,马达之间的合作结合定量地解释了实验中观察到的聚集现象。沿 MT 的长度的合作结合以及在尖端后面的距离处的成核点定义了回收周期。基于数值结果和实验数据的比较,我们估计了一个合作结合概率和浓度范围,在此范围内会发生回收现象。