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引用本文的文献

1
Restoration of cytoskeletal and membrane tethering defects but not defects in membrane trafficking in the intestinal brush border of mice lacking both myosin Ia and myosin VI.在同时缺乏肌球蛋白Ia和肌球蛋白VI的小鼠的肠道刷状缘中,细胞骨架和膜系留缺陷得以恢复,但膜运输缺陷未得到恢复。
Cytoskeleton (Hoboken). 2015 Sep;72(9):455-76. doi: 10.1002/cm.21238. Epub 2015 Sep 16.
2
Myosin motors at neuronal synapses: drivers of membrane transport and actin dynamics.神经元突触处的肌球蛋白马达:膜转运和肌动蛋白动力学的驱动器。
Nat Rev Neurosci. 2013 Apr;14(4):233-47. doi: 10.1038/nrn3445. Epub 2013 Mar 13.

本文引用的文献

1
Myosin Va and myosin VI coordinate their steps while engaged in an in vitro tug of war during cargo transport.肌球蛋白 Va 和肌球蛋白 VI 在体外货物运输拔河比赛中协调它们的步伐。
Proc Natl Acad Sci U S A. 2011 Aug 23;108(34):E535-41. doi: 10.1073/pnas.1104298108. Epub 2011 Aug 1.
2
Extension of a three-helix bundle domain of myosin VI and key role of calmodulins.肌球蛋白 VI 的三螺旋束结构域的扩展及其钙调蛋白的关键作用。
Biophys J. 2011 Jun 22;100(12):2964-73. doi: 10.1016/j.bpj.2011.05.010.
3
Multifunctional myosin VI has a multitude of cargoes.多功能肌球蛋白VI有多种货物。
Proc Natl Acad Sci U S A. 2011 Apr 12;108(15):5927-8. doi: 10.1073/pnas.1103086108. Epub 2011 Apr 4.
4
Robust mechanosensing and tension generation by myosin VI.肌球蛋白 VI 的稳健机械感知和张力产生。
J Mol Biol. 2011 Jan 7;405(1):105-12. doi: 10.1016/j.jmb.2010.10.010. Epub 2010 Oct 21.
5
Myosin VI and optineurin are required for polarized EGFR delivery and directed migration.肌球蛋白 VI 和视神经萎缩症相关蛋白是极化 EGFR 运输和定向迁移所必需的。
Traffic. 2010 Oct;11(10):1290-303. doi: 10.1111/j.1600-0854.2010.01101.x.
6
Differential localization and dynamics of class I myosins in the enterocyte microvillus.I 类肌球蛋白在肠上皮细胞微绒毛中的差异定位和动力学。
Mol Biol Cell. 2010 Mar 15;21(6):970-8. doi: 10.1091/mbc.e09-07-0638. Epub 2010 Jan 20.
7
Myosin isoform determines the conformational dynamics and cooperativity of actin filaments in the strongly bound actomyosin complex.肌球蛋白同工型决定了强结合肌球蛋白复合物中肌动蛋白丝的构象动力学和协同性。
J Mol Biol. 2010 Feb 26;396(3):501-9. doi: 10.1016/j.jmb.2009.11.063. Epub 2009 Dec 4.
8
Combining single-molecule optical trapping and small-angle x-ray scattering measurements to compute the persistence length of a protein ER/K alpha-helix.将单分子光阱和小角 X 射线散射测量相结合,计算 ER/K 螺旋蛋白的持久长度。
Biophys J. 2009 Dec 2;97(11):2993-9. doi: 10.1016/j.bpj.2009.09.009.
9
Cargo binding induces dimerization of myosin VI.货物结合诱导肌球蛋白VI二聚化。
Proc Natl Acad Sci U S A. 2009 Oct 13;106(41):17320-4. doi: 10.1073/pnas.0909748106. Epub 2009 Sep 28.
10
Potential roles of myosin VI in cell motility.肌球蛋白VI在细胞运动中的潜在作用。
Biochem Soc Trans. 2009 Oct;37(Pt 5):966-70. doi: 10.1042/BST0370966.

正向末端肌球蛋白推动肌动蛋白丝滑动由单头肌球蛋白 VI 完成。

Plus-end directed myosins accelerate actin filament sliding by single-headed myosin VI.

机构信息

Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520-8103, USA.

出版信息

Cytoskeleton (Hoboken). 2012 Jan;69(1):59-69. doi: 10.1002/cm.21002. Epub 2012 Jan 9.

DOI:10.1002/cm.21002
PMID:22213699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3327287/
Abstract

Myosin VI (Myo6) is unique among myosins in that it moves toward the minus (pointed) end of the actin filament. Thus to exert tension on, or move cargo along an actin filament, Myo6 is working against potentially multiple plus (barbed)-end myosins. To test the effect of plus-end motors on Myo6, the gliding actin filament assay was used to assess the motility of single-headed Myo6 in the absence and presence of cardiac myosin II (Myo2) and myosin Va (Myo5a). Myo6 alone exhibited a filament gliding velocities of 60.34 ± 13.68 nm/s. Addition of either Myo2 or Myo5a, at densities below that required to promote plus-end movement resulted in an increase in Myo6 velocity (~100-150% increase). Movement in the presence of these plus-end myosins was minus-end directed as determined using polarity tagged filaments. High densities of Myo2 or Myo5a were required to convert to plus-end directed motility indicating that Myo6 is a potent inhibitor of Myo2 and Myo5a. Previous studies have shown that two-headed Myo6 slows and then stalls in an anchored state under load. Consistent with these studies, velocity of a two headed heavy mero myosin form of Myo6 was unaffected by Myo5a at low densities, and was inhibited at high Myo5a densities.

摘要

肌球蛋白 VI(Myo6)在肌球蛋白家族中是独一无二的,因为它朝着肌动蛋白丝的负(指向)端移动。因此,为了对肌动蛋白丝施加张力或沿肌动蛋白丝移动货物,Myo6 必须与多个正(棘突)端肌球蛋白对抗。为了测试正端马达对 Myo6 的影响,使用滑行肌动蛋白丝测定法来评估在不存在和存在心脏肌球蛋白 II(Myo2)和肌球蛋白 Va(Myo5a)的情况下,单头 Myo6 的运动。Myo6 单独表现出 60.34 ± 13.68nm/s 的丝状滑行速度。添加密度低于促进正端运动所需密度的 Myo2 或 Myo5a 会导致 Myo6 速度增加(约增加 100-150%)。使用极性标记的丝来确定,在这些正端肌球蛋白存在的情况下,运动是负端定向的。需要高浓度的 Myo2 或 Myo5a 才能转化为正端定向运动,表明 Myo6 是 Myo2 和 Myo5a 的有效抑制剂。先前的研究表明,双头 Myo6 在负载下会减慢并随后停滞在固定状态。与这些研究一致,低浓度的 Myo5a 对双头重肌球蛋白形式的 Myo6 的速度没有影响,而在高 Myo5a 浓度下则受到抑制。