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Single-Molecule Studies of Protein Folding with Optical Tweezers.
Annual Review of Biochemistry ( IF 12.1 ) Pub Date : 2020-06-22 , DOI: 10.1146/annurev-biochem-013118-111442
Carlos Bustamante 1, 2 , Lisa Alexander 2 , Kevin Maciuba 3 , Christian M Kaiser 4
Affiliation  

Manipulation of individual molecules with optical tweezers provides a powerful means of interrogating the structure and folding of proteins. Mechanical force is not only a relevant quantity in cellular protein folding and function, but also a convenient parameter for biophysical folding studies. Optical tweezers offer precise control in the force range relevant for protein folding and unfolding, from which single-molecule kinetic and thermodynamic information about these processes can be extracted. In this review, we describe both physical principles and practical aspects of optical tweezers measurements and discuss recent advances in the use of this technique for the study of protein folding. In particular, we describe the characterization of folding energy landscapes at high resolution, studies of structurally complex multidomain proteins, folding in the presence of chaperones, and the ability to investigate real-time cotranslational folding of a polypeptide.

中文翻译:



用光镊进行蛋白质折叠的单分子研究。



用光镊操作单个分子提供了一种研究蛋白质结构和折叠的强大方法。机械力不仅是细胞蛋白质折叠和功能的相关量,也是生物物理折叠研究的便利参数。光镊可以精确控制与蛋白质折叠和展开相关的力范围,从中可以提取有关这些过程的单分子动力学和热力学信息。在这篇综述中,我们描述了光镊测量的物理原理和实际方面,并讨论了使用该技术研究蛋白质折叠的最新进展。特别是,我们描述了高分辨率折叠能量景观的表征、结构复杂的多域蛋白质的研究、分子伴侣存在下的折叠以及研究多肽的实时共翻译折叠的能力。

更新日期:2020-06-23
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