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对HtrI转导器上与感官视紫红质I相互作用的位点进行缺失作图。

Deletion mapping of the sites on the HtrI transducer for sensory rhodopsin I interaction.

作者信息

Perazzona B, Spudich E N, Spudich J L

机构信息

Department of Microbiology and Molecular Genetics, University of Texas-Houston Health Science Center 77030, USA.

出版信息

J Bacteriol. 1996 Nov;178(22):6475-8. doi: 10.1128/jb.178.22.6475-6478.1996.

DOI:10.1128/jb.178.22.6475-6478.1996
PMID:8932303
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC178533/
Abstract

The phototaxis receptor sensory rhodopsin I (SRI) transmits signals through a membrane-bound transducer protein, HtrI. The genes for the receptor and transducer, sopI and htrI, respectively, are normally cotranscribed; however, previous work has established that fully functional interacting proteins are produced when htrI is expressed from the chromosome and sopI is expressed from a different promoter on a plasmid. In this report we show that in the membrane, concentrations of SRI from plasmid expression of wild-type sopI are negligible in the absence of HtrI protein in the cell. This requirement for HtrI is eliminated when sopI is extended at the 5'-end with 63 nucleotides of the bop gene, which encodes the N-terminal signal sequence of the bacteriorhodopsin protein. The signal is cleaved from the chimeric protein, and processed SRI is stable in the HtrI-free membrane. These results suggest a chaperone-like function for HtrI that facilitates membrane insertion or proper folding of the SRI protein. Six deletion constructs of HtrI were examined to localize the interaction sites for its putative chaperone function and for HtrI control of the SRI photocycle, a phenomenon described previously. The smallest HtrI fragment identified, which contained interaction sites for both SRI stability and photocycle control, consisted of the N-terminal 147 residues of the 536-residue HtrI protein. The active fragment is predicted to contain two transmembrane helices and the first approximately 20% of the cytoplasmic portion of the protein.

摘要

趋光性受体感官视紫红质I(SRI)通过膜结合转导蛋白HtrI传递信号。受体基因和转导蛋白基因分别为sopI和htrI,通常共转录;然而,先前的研究表明,当htrI从染色体表达,sopI从质粒上的不同启动子表达时,会产生功能完全正常的相互作用蛋白。在本报告中,我们表明,在细胞膜中,当细胞中不存在HtrI蛋白时,野生型sopI质粒表达产生的SRI浓度可忽略不计。当sopI在5'端延伸63个编码细菌视紫红质蛋白N端信号序列的bop基因核苷酸时,对HtrI的这种需求就消除了。信号从嵌合蛋白上切割下来,加工后的SRI在无HtrI的膜中稳定存在。这些结果表明HtrI具有类似伴侣蛋白的功能,可促进SRI蛋白的膜插入或正确折叠。我们检测了HtrI的六个缺失构建体,以定位其假定伴侣功能的相互作用位点以及HtrI对SRI光循环的控制位点,这是一种先前描述过的现象。鉴定出的最小HtrI片段包含SRI稳定性和光循环控制的相互作用位点,由536个氨基酸的HtrI蛋白的N端147个残基组成。预测该活性片段包含两个跨膜螺旋和该蛋白约20%的细胞质部分。

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Deletion mapping of the sites on the HtrI transducer for sensory rhodopsin I interaction.对HtrI转导器上与感官视紫红质I相互作用的位点进行缺失作图。
J Bacteriol. 1996 Nov;178(22):6475-8. doi: 10.1128/jb.178.22.6475-6478.1996.
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本文引用的文献

1
Protonatable residues at the cytoplasmic end of transmembrane helix-2 in the signal transducer HtrI control photochemistry and function of sensory rhodopsin I.信号转导蛋白HtrI中跨膜螺旋2胞质端的可质子化残基控制着感官视紫红质I的光化学和功能。
Proc Natl Acad Sci U S A. 1996 Jun 25;93(13):6557-61. doi: 10.1073/pnas.93.13.6557.
2
Molecular mechanism of transmembrane signaling by the aspartate receptor: a model.天冬氨酸受体介导跨膜信号传导的分子机制:一种模型
Proc Natl Acad Sci U S A. 1996 Mar 19;93(6):2545-50. doi: 10.1073/pnas.93.6.2545.
3
Synthesis of a gene for sensory rhodopsin I and its functional expression in Halobacterium halobium.感官视紫红质I基因的合成及其在嗜盐菌中的功能表达。
Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3486-90. doi: 10.1073/pnas.90.8.3486.
4
The photochemical reactions of sensory rhodopsin I are altered by its transducer.感官视紫红质I的光化学反应会被其转导器改变。
J Biol Chem. 1993 Aug 5;268(22):16095-7.
5
Color sensing in the Archaea: a eukaryotic-like receptor coupled to a prokaryotic transducer.古菌中的颜色感知:一种与原核生物转导器偶联的类真核生物受体。
J Bacteriol. 1993 Dec;175(24):7755-61. doi: 10.1128/jb.175.24.7755-7761.1993.
6
Protein-protein interaction converts a proton pump into a sensory receptor.蛋白质-蛋白质相互作用将质子泵转化为感觉受体。
Cell. 1994 Dec 2;79(5):747-50. doi: 10.1016/0092-8674(94)90064-7.
7
Identification of distinct domains for signaling and receptor interaction of the sensory rhodopsin I transducer, HtrI.鉴定感官视紫红质I转导蛋白HtrI的信号传导和受体相互作用的不同结构域。
J Bacteriol. 1994 Nov;176(22):6931-5. doi: 10.1128/jb.176.22.6931-6935.1994.
8
A cytoplasmic domain is required for the functional interaction of SRI and HtrI in archaeal signal transduction.在古细菌信号转导中,SRI和HtrI的功能相互作用需要一个细胞质结构域。
FEBS Lett. 1994 Oct 24;353(3):301-4. doi: 10.1016/0014-5793(94)01068-4.
9
Chemotaxis and phototaxis require a CheA histidine kinase in the archaeon Halobacterium salinarium.趋化性和趋光性需要嗜盐古菌盐生盐杆菌中的一种CheA组氨酸激酶。
EMBO J. 1995 Feb 15;14(4):667-73. doi: 10.1002/j.1460-2075.1995.tb07045.x.
10
Lock on/off disulfides identify the transmembrane signaling helix of the aspartate receptor.锁定/解锁二硫键可确定天冬氨酸受体的跨膜信号螺旋结构。
J Biol Chem. 1995 Oct 13;270(41):24043-53. doi: 10.1074/jbc.270.41.24043.