Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Uttar Pradesh, India.
Eur Biophys J. 2011 May;40(5):611-7. doi: 10.1007/s00249-010-0658-z. Epub 2011 Jan 4.
In recent years, many advances have been made in the understanding of functional and structural characteristics of protein evolution from denaturant-based studies that subject the protein to a change in the microenvironment. This paper reports the chemical denaturation of purified goat muscle cystatin (GMC) a thiol-proteinase inhibitor, using urea and guanidine hydrochloride (GdnHCl). The subtle conformational changes of GMC were monitored by intrinsic fluorescence, extrinsic fluorescence, and CD spectroscopic techniques. Further, the activity of GMC as a function of increasing concentration of denaturants was also studied. It was found that increasing the concentration of GdnHCl significantly enhances the inactivation and unfolding of the inhibitor (GMC). In urea-induced denaturation, the intrinsic and extrinsic fluorescence intensity reveals significant structural changes in the inhibitor. Further, it was found that at low concentrations of urea, up to 0.5-1.0 M: , there was quenching of fluorescence intensity compared with the native form and a red shift of 5 nm was observed up to 5-8 M: . The results presented in this paper suggest that GdnHCl-induced denaturation of GMC follows a simple two-state rule in which native → denatured state transition occurs in a single step. However denaturation with urea proceeds through an intermediate or non-native state.
近年来,通过基于变性剂的研究,人们对蛋白质进化的功能和结构特征有了更多的了解,这些研究使蛋白质的微环境发生了变化。本文报道了用脲和盐酸胍(GdnHCl)对纯化的山羊肌肉半胱氨酸蛋白酶抑制剂(GMC)进行化学变性。通过内源荧光、外源荧光和 CD 光谱技术监测 GMC 的细微构象变化。此外,还研究了 GMC 作为变性剂浓度增加的函数的活性。结果发现,增加 GdnHCl 的浓度显著增强了抑制剂(GMC)的失活和展开。在脲诱导的变性中,抑制剂的内源和外源荧光强度显示出明显的结构变化。此外,发现低浓度脲(0.5-1.0 M)时,与天然形式相比,荧光强度猝灭,并且在 5-8 M 时观察到 5nm 的红移:。本文的结果表明,GdnHCl 诱导的 GMC 变性遵循简单的两态规则,其中天然状态到变性状态的转变发生在一个步骤中。然而,脲变性是通过中间态或非天然态进行的。