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光活性黄色蛋白中的信号转导。I. 光子吸收与发色团异构化

Signal transduction in the photoactive yellow protein. I. Photon absorption and the isomerization of the chromophore.

作者信息

Groenhof Gerrit, Lensink Marc F, Berendsen Herman J C, Snijders Jaap G, Mark Alan E

机构信息

Department of Biophysical Chemistry, Groningen Biomolecular Sciences and Biotechnology Institute, Rijksuniversiteit Groningen, Groningen, The Netherlands.

出版信息

Proteins. 2002 Aug 1;48(2):202-11. doi: 10.1002/prot.10136.

Abstract

Molecular dynamics simulation techniques together with time-dependent density functional theory calculations have been used to investigate the effect of photon absorption by a 4-hydroxy-cinnamic acid chromophore on the structural properties of the photoactive yellow protein (PYP) from Ectothiorodospira halophila. The calculations suggest that the protein not only modifies the absorption spectrum of the chromophore but also regulates the subsequent isomerization of the chromophore by stabilizing the isomerization transition state. Although signaling from PYP is thought to involve partial unfolding of the protein, the mechanical effects accompanying isomerization do not appear to directly destabilize the protein.

摘要

分子动力学模拟技术与含时密度泛函理论计算相结合,用于研究4-羟基肉桂酸发色团吸收光子对嗜盐外硫红螺菌光活性黄色蛋白(PYP)结构性质的影响。计算结果表明,该蛋白不仅改变了发色团的吸收光谱,还通过稳定异构化过渡态来调节发色团随后的异构化过程。尽管人们认为PYP发出信号涉及蛋白质的部分解折叠,但异构化伴随的力学效应似乎并未直接使蛋白质不稳定。

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