Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, WI 53706, USA.
Methods. 2010 Sep;52(1):57-73. doi: 10.1016/j.ymeth.2010.06.001. Epub 2010 Jun 8.
Protein folding is a fundamental biological process of great significance for cell function and life-related processes. Surprisingly, very little is presently known about how proteins fold in vivo. The influence of the cellular environment is of paramount importance, as molecular chaperones, the ribosome, and the crowded medium affect both folding pathways and potentially even equilibrium structures. Studying protein folding in physiologically relevant environments, however, poses a number of technical challenges due to slow tumbling rates, low concentrations and potentially non-homogenous populations. Early work in this area relied on biological assays based on antibody recognition, proteolysis, and activity studies. More recently, it has been possible to directly observe the structure and dynamics of nascent polypeptides at high resolution by spectroscopic and microscopic techniques. The fluorescence depolarization decay of nascent polypeptides labeled with a small extrinsic fluorophore is a particularly powerful tool to gain insights into the dynamics of newly synthesized proteins. The fluorophore label senses both its own local mobility and the motions of the macromolecule to which it is attached. Fluorescence anisotropy decays can be measured both in the time and frequency domains. The latter mode of data collection is extremely convenient to capture the nanosecond motions in ribosome-bound nascent proteins, indicative of the development of independent structure and folding on the ribosome. In this review, we discuss the theory of fluorescence depolarization and its exciting applications to the study of the dynamics of nascent proteins in the cellular environment.
蛋白质折叠是一个非常重要的生物学过程,对细胞功能和与生命相关的过程都有重要意义。令人惊讶的是,目前对于蛋白质在体内是如何折叠的知之甚少。细胞环境的影响至关重要,因为分子伴侣、核糖体和拥挤的介质会影响折叠途径,甚至可能影响平衡结构。然而,由于旋转速率慢、浓度低以及潜在的非均相群体等原因,在生理相关环境中研究蛋白质折叠存在许多技术挑战。在这一领域的早期工作依赖于基于抗体识别、蛋白水解和活性研究的生物测定。最近,通过光谱和显微镜技术,已经可以直接观察到新生多肽的结构和动力学,达到高分辨率。用小的外源性荧光团标记的新生多肽的荧光各向异性衰减是一种特别强大的工具,可以深入了解新合成蛋白质的动力学。荧光团标记既能感知自身的局部流动性,也能感知与其相连的大分子的运动。荧光各向异性衰减可以在时间域和频率域中进行测量。后一种数据采集模式非常方便,可以捕获核糖体结合的新生蛋白质中的纳秒运动,这表明核糖体上独立结构和折叠的发展。在这篇综述中,我们讨论了荧光各向异性衰减的理论及其在研究细胞环境中新生蛋白质动力学方面的令人兴奋的应用。