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Procoat是M13外壳蛋白的前体,其插入膜中需要电化学势。

Procoat, the precursor of M13 coat protein, requires an electrochemical potential for membrane insertion.

作者信息

Date T, Goodman J M, Wickner W T

出版信息

Proc Natl Acad Sci U S A. 1980 Aug;77(8):4669-73. doi: 10.1073/pnas.77.8.4669.

DOI:10.1073/pnas.77.8.4669
PMID:7001463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC349907/
Abstract

The coat protein of coliphage M13 spans the host cell cytoplasmic membrane prior to its assembly into extruding virus. It is made as a soluble cytoplasmic precursor, termed "procoat," with 23 extra amino acid residues at the NH2 terminus. Procoat binds to the cell membrane and is converted proteolytically to coat protein. When the electrochemical gradient of an infected cell is rapidly dissipated by uncouplers, procoat still binds to the plasma membrane but is not converted to coat. We report here that membrane-bound procoat is only detected at the inner face of the cytoplasmic membrane and that uncouplers prevent it from integrating into a transmembrane conformation.

摘要

大肠杆菌噬菌体M13的外壳蛋白在组装成出芽病毒之前跨越宿主细胞质膜。它最初作为一种可溶性细胞质前体产生,称为“前衣壳”,在NH2末端有23个额外的氨基酸残基。前衣壳与细胞膜结合,并通过蛋白水解作用转化为外壳蛋白。当感染细胞的电化学梯度被解偶联剂迅速消散时,前衣壳仍与质膜结合,但不会转化为外壳蛋白。我们在此报告,膜结合的前衣壳仅在细胞质膜的内表面被检测到,并且解偶联剂阻止它整合到跨膜构象中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/040cf4a71fcb/pnas00495-0294-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/cfe2fd05acec/pnas00495-0292-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/0bc05618aca5/pnas00495-0292-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/8506dd750a45/pnas00495-0292-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/6ae97b74d1c1/pnas00495-0292-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/e790f230d571/pnas00495-0292-e.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/8a09518d0877/pnas00495-0292-f.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/306fac3a7229/pnas00495-0293-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/dd2c0932a9bf/pnas00495-0293-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/040cf4a71fcb/pnas00495-0294-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/cfe2fd05acec/pnas00495-0292-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/0bc05618aca5/pnas00495-0292-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/8506dd750a45/pnas00495-0292-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/6ae97b74d1c1/pnas00495-0292-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/e790f230d571/pnas00495-0292-e.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/8a09518d0877/pnas00495-0292-f.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/306fac3a7229/pnas00495-0293-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/dd2c0932a9bf/pnas00495-0293-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec9/349907/040cf4a71fcb/pnas00495-0294-a.jpg

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Procoat, the precursor of M13 coat protein, requires an electrochemical potential for membrane insertion.Procoat是M13外壳蛋白的前体,其插入膜中需要电化学势。
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4669-73. doi: 10.1073/pnas.77.8.4669.
2
Mechanisms of membrane assembly: effects of energy poisons on the conversion of soluble M13 coliphage procoat to membrane-bound coat protein.膜组装机制:能量毒物对可溶性M13噬菌体原衣壳转化为膜结合衣壳蛋白的影响。
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Soluble precursor of an integral membrane protein: synthesis of procoat protein in Escherichia coli infected with bacteriophage M13.整合膜蛋白的可溶性前体:感染噬菌体M13的大肠杆菌中前衣壳蛋白的合成。
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本文引用的文献

1
Synthesis, assembly into the cytoplasmic membrane, and proteolytic processing of the precursor of coliphage M13 coat protein.大肠杆菌噬菌体M13外壳蛋白前体的合成、组装到细胞质膜以及蛋白水解加工
J Biol Chem. 1980 Mar 10;255(5):2123-30.
2
Mechanisms of membrane assembly: effects of energy poisons on the conversion of soluble M13 coliphage procoat to membrane-bound coat protein.膜组装机制:能量毒物对可溶性M13噬菌体原衣壳转化为膜结合衣壳蛋白的影响。
Proc Natl Acad Sci U S A. 1980 Feb;77(2):827-31. doi: 10.1073/pnas.77.2.827.
3
[Virus proteins. IV. Constitution of the coat protein of the fd phage].
Res Microbiol. 2013 Jul-Aug;164(6):497-504. doi: 10.1016/j.resmic.2013.03.007. Epub 2013 Mar 26.
4
Spatial expression of the genome: the signal hypothesis at forty.基因组的空间表达:信号假说四十年。
Nat Rev Mol Cell Biol. 2011 May;12(5):333-40. doi: 10.1038/nrm3105. Epub 2011 Apr 13.
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Mechanism and hydrophobic forces driving membrane protein insertion of subunit II of cytochrome bo 3 oxidase.细胞色素bo 3氧化酶亚基II膜蛋白插入的机制及疏水作用力
J Mol Biol. 2008 Feb 1;375(5):1282-92. doi: 10.1016/j.jmb.2007.11.054. Epub 2007 Nov 22.
6
F1F0 ATP synthase subunit c is a substrate of the novel YidC pathway for membrane protein biogenesis.F1F0 ATP合酶亚基c是膜蛋白生物合成新的YidC途径的一个底物。
J Cell Biol. 2004 Apr 26;165(2):213-22. doi: 10.1083/jcb.200402100. Epub 2004 Apr 19.
7
The SecA subunit of Escherichia coli preprotein translocase is exposed to the periplasm.大肠杆菌前体蛋白转位酶的SecA亚基暴露于周质中。
J Bacteriol. 1998 Nov;180(21):5776-9. doi: 10.1128/JB.180.21.5776-5779.1998.
8
In vivo membrane assembly of the E.coli polytopic protein, melibiose permease, occurs via a Sec-independent process which requires the protonmotive force.大肠杆菌多聚体蛋白蜜二糖通透酶的体内膜组装通过一种不依赖Sec的过程发生,该过程需要质子动力。
EMBO J. 1996 Oct 1;15(19):5202-8.
9
Similarity between the 38-kilodalton lipoprotein of Treponema pallidum and the glucose/galactose-binding (MglB) protein of Escherichia coli.梅毒螺旋体38千道尔顿脂蛋白与大肠杆菌葡萄糖/半乳糖结合蛋白(MglB)之间的相似性。
Infect Immun. 1994 Apr;62(4):1381-91. doi: 10.1128/iai.62.4.1381-1391.1994.
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6
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7
Orientation of membrane vesicles from Escherichia coli prepared by different procedures.通过不同程序制备的来自大肠杆菌的膜囊泡的取向。
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Asymmetric orientation of phage M13 coat protein in Escherichia coli cytoplasmic membranes and in synthetic lipid vesicles.噬菌体M13外壳蛋白在大肠杆菌细胞质膜和合成脂质囊泡中的不对称取向。
Proc Natl Acad Sci U S A. 1976 Apr;73(4):1159-63. doi: 10.1073/pnas.73.4.1159.