Fontana A, Polverino de Laureto P, De Filippis V, Scaramella E, Zambonin M
CRIBI Biotechnology Centre, University of Padua, Italy.
Fold Des. 1997;2(2):R17-26. doi: 10.1016/S1359-0278(97)00010-2.
The folding of a polypeptide chain of a relatively large globular protein into its unique three-dimensional and functionally active structure occurs via folding intermediates. These partly folded states of proteins are difficult to characterize, because they are usually short lived or exist as a distribution of possible conformers. A variety of experimental techniques and approaches have been utilized in recent years in numerous laboratories for characterizing folding intermediates that occur at equilibrium, including spectroscopic techniques, solution X-ray scattering, calorimetry and gel filtration chromatography, as well as genetic methods and theoretical calculations. In this review, we focus on the use of proteolytic enzymes as probes of the structure and dynamics of folding intermediates and we show that this simple biochemical technique can provide useful information, complementing that obtained by other commonly used techniques and approaches. The key result of the proteolysis experiments is that partly folded states (molten globules) of proteins can be sufficiently rigid to prevent extensive proteolysis and appear to maintain significant native-like structure.
相对较大的球状蛋白质的多肽链折叠成其独特的三维功能活性结构是通过折叠中间体实现的。蛋白质的这些部分折叠状态很难表征,因为它们通常寿命短暂,或者以可能构象的分布形式存在。近年来,众多实验室采用了各种实验技术和方法来表征处于平衡状态的折叠中间体,包括光谱技术、溶液X射线散射、量热法和凝胶过滤色谱法,以及遗传学方法和理论计算。在本综述中,我们重点关注使用蛋白水解酶作为折叠中间体结构和动力学的探针,并表明这种简单的生化技术可以提供有用信息,补充通过其他常用技术和方法获得的信息。蛋白水解实验的关键结果是,蛋白质的部分折叠状态(熔球态)可以足够刚性以防止广泛的蛋白水解,并且似乎保持显著的类天然结构。