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驱动蛋白的靶向作用。

Targeting of motor proteins.

作者信息

Vallee R B, Sheetz M P

机构信息

Worcester Foundation for Biomedical Research, Shrewsbury, MA 01545, USA.

出版信息

Science. 1996 Mar 15;271(5255):1539-44. doi: 10.1126/science.271.5255.1539.

DOI:10.1126/science.271.5255.1539
PMID:8599110
Abstract

Microtubules are responsible for chromosome segregation and the movement and reorganization of membranous organelles. Many aspects of microtubule-based motility can be attributed to the action of motor proteins, producing force directed toward either end of microtubules. How these proteins are targeted to the appropriate organellar sites within the cell, however, has remained a mystery. Recent work has begun to define the targeting mechanism for two well-studied motor proteins, kinesin and cytoplasmic dynein.

摘要

微管负责染色体分离以及膜性细胞器的移动和重组。基于微管的运动的许多方面可归因于驱动蛋白的作用,产生朝向微管两端的力。然而,这些蛋白质如何靶向细胞内合适的细胞器位点仍是个谜。最近的研究已开始明确两种经过充分研究的驱动蛋白——驱动蛋白和胞质动力蛋白的靶向机制。

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1
Targeting of motor proteins.驱动蛋白的靶向作用。
Science. 1996 Mar 15;271(5255):1539-44. doi: 10.1126/science.271.5255.1539.
2
Targeting of cytoplasmic dynein to membranous organelles and kinetochores via dynactin.通过动力蛋白激活蛋白将胞质动力蛋白靶向至膜性细胞器和动粒。
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Kinesin and dynein superfamily proteins and the mechanism of organelle transport.驱动蛋白和动力蛋白超家族蛋白与细胞器运输机制
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4
Dynein, dynactin, and kinesin II's interaction with microtubules is regulated during bidirectional organelle transport.在双向细胞器运输过程中,动力蛋白、动力蛋白激活蛋白和驱动蛋白II与微管的相互作用受到调控。
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Functional analysis of dynactin and cytoplasmic dynein in slow axonal transport.动力蛋白激活蛋白和胞质动力蛋白在轴突慢速运输中的功能分析
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Accumulation of cytoplasmic dynein and dynactin at microtubule plus ends in Aspergillus nidulans is kinesin dependent.在构巢曲霉中,细胞质动力蛋白和动力蛋白激活蛋白在微管正端的积累依赖于驱动蛋白。
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J Cell Biol. 1996 May;133(3):585-93. doi: 10.1083/jcb.133.3.585.

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