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非洲爪蟾驱动蛋白II异源三聚体复合物的一个亚基xklp3在内质网与高尔基体之间的膜转运中的作用。

Role of xklp3, a subunit of the Xenopus kinesin II heterotrimeric complex, in membrane transport between the endoplasmic reticulum and the Golgi apparatus.

作者信息

Le Bot N, Antony C, White J, Karsenti E, Vernos I

机构信息

Cell Biology and Biophysics Program, European Molecular Biological Laboratory, D-69117 Heidelberg, Germany.

出版信息

J Cell Biol. 1998 Dec 14;143(6):1559-73. doi: 10.1083/jcb.143.6.1559.

Abstract

The function of the Golgi apparatus is to modify proteins and lipids synthesized in the ER and sort them to their final destination. The steady-state size and function of the Golgi apparatus is maintained through the recycling of some components back to the ER. Several lines of evidence indicate that the spatial segregation between the ER and the Golgi apparatus as well as trafficking between these two compartments require both microtubules and motors. We have cloned and characterized a new Xenopus kinesin like protein, Xklp3, a subunit of the heterotrimeric Kinesin II. By immunofluorescence it is found in the Golgi region. A more detailed analysis by EM shows that it is associated with a subset of membranes that contain the KDEL receptor and are localized between the ER and Golgi apparatus. An association of Xklp3 with the recycling compartment is further supported by a biochemical analysis and the behavior of Xklp3 in BFA-treated cells. The function of Xklp3 was analyzed by transfecting cells with a dominant-negative form lacking the motor domain. In these cells, the normal delivery of newly synthesized proteins to the Golgi apparatus is blocked. Taken together, these results indicate that Xklp3 is involved in the transport of tubular-vesicular elements between the ER and the Golgi apparatus.

摘要

高尔基体的功能是修饰在内质网中合成的蛋白质和脂质,并将它们分类到最终目的地。高尔基体的稳态大小和功能通过将一些成分循环回内质网来维持。几条证据表明,内质网和高尔基体之间的空间分隔以及这两个区室之间的运输需要微管和马达蛋白。我们已经克隆并鉴定了一种新的非洲爪蟾类驱动蛋白样蛋白Xklp3,它是异源三聚体驱动蛋白II的一个亚基。通过免疫荧光发现它存在于高尔基体区域。通过电子显微镜进行的更详细分析表明,它与一组含有KDEL受体且位于内质网和高尔基体之间的膜相关联。Xklp3与再循环区室的关联进一步得到生化分析以及Xklp3在经BFA处理的细胞中的行为的支持。通过用缺乏马达结构域的显性负性形式转染细胞来分析Xklp3的功能。在这些细胞中,新合成蛋白质向高尔基体的正常运输被阻断。综上所述,这些结果表明Xklp3参与内质网和高尔基体之间管状小泡成分的运输。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b2/2132969/104fa5445825/JCB9808066.f1a.jpg

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