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Single-Molecule Studies of Protein Folding with Optical Tweezers

机译:用光学镊子折叠蛋白质的单分子研究

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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.
机译:用光学镊子操纵单个分子提供了询问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,而且是生物物理折叠研究的方便参数。 光学镊子在与蛋白质折叠和展开相关的力范围内提供精确控制,可以从中提取关于这些过程的单分子动力学和热力学信息。 在本文中,我们描述了光学镊子测量的物理原则和实践方面,并讨论了这种技术用于研究蛋白质折叠的研究的最新进展。 特别是,我们描述了高分辨率折叠能量景观的表征,在结构上复杂的多域蛋白质的研究,在伴侣存在下折叠,以及研究多肽的实时分键折叠的能力。

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