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静电相互作用对体内伴侣蛋白与客户蛋白的相互作用很重要。

Electrostatic interactions are important for chaperone-client interaction in vivo.

作者信息

Lee Changhan, Kim Hyunhee, Bardwell James C A

机构信息

Department of Molecular, Cellular, and Developmental Biology, Howard Hughes Medical Institute, University of Michigan, Ann Arbor, MI, USA.

出版信息

Microbiology (Reading). 2018 Jul;164(7):992-997. doi: 10.1099/mic.0.000676. Epub 2018 Jun 5.

Abstract

It has long been thought that chaperones are primarily attracted to their clients through the hydrophobic effect. However, in in vitro studies on the interaction between the chaperone Spy and its substrate Im7, we recently showed that long-range electrostatic interactions also play a key role. Spy functions in the periplasm of Gram-negative bacteria, which is surrounded by a permeable outer membrane. The ionic conditions in the periplasm therefore closely mimic those in the media, which allowed us to vary the ionic strength of the in vivo folding environment. Using folding biosensors that link protein folding to antibiotic resistance, we were able to monitor Spy chaperone activity in Escherichia coli in vivo as a function of media salt concentration. The chaperone activity of Spy decreased when the ionic strength of the media was increased, strongly suggesting that electrostatic forces play a vital role in the action of Spy in vivo.

摘要

长期以来,人们一直认为伴侣蛋白主要通过疏水作用吸引其底物。然而,最近我们在关于伴侣蛋白Spy与其底物Im7相互作用的体外研究中表明,长程静电相互作用也起着关键作用。Spy在革兰氏阴性菌的周质中发挥作用,周质被一层可渗透的外膜包围。因此,周质中的离子条件与培养基中的离子条件非常相似,这使我们能够改变体内折叠环境的离子强度。使用将蛋白质折叠与抗生素抗性联系起来的折叠生物传感器,我们能够监测大肠杆菌体内Spy伴侣蛋白的活性随培养基盐浓度的变化。当培养基的离子强度增加时,Spy的伴侣蛋白活性降低,这有力地表明静电力在Spy体内的作用中起着至关重要的作用。

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