Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, India.
Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, India.
Arch Biochem Biophys. 2014 Nov 15;562:51-61. doi: 10.1016/j.abb.2014.08.015. Epub 2014 Aug 28.
Conformational alterations and aggregates of chickpea cystatin (CPC) were investigated upon sequential addition of trifluoroethanol (TFE) over a range of 0-70% v/v. CPC on 30% and 40% v/v TFE addition exhibited non-native β-sheet, altered intrinsic fluorescence, increased thioflavin T fluorescence, prominent red shifted shoulder peak in Congo red absorbance, and enhanced turbidity as well as Rayleigh scattering, suggesting the aggregate formation. TEM results confirmed the formation of fibrillar aggregates at 30% and 40% v/v TFE. On increasing concentration of TFE to 70% v/v, CPC showed retention of native-like secondary structure, increased intrinsic and ANS fluorescence. Thus our results show that favourable condition for fibrillation of CPC is in the range of 30-40% TFE. Moreover, anti-aggregational effects of polyphenols, epicatechin (EC) and tannic acid (TA) were analysed using ThT binding assay and other biophysical assays. EC and TA produced a concentration dependent decline in ThT fluorescence suggesting inhibition of the fibril formation. Furthermore, TA in comparison to EC, served as a more effective inhibitor against amyloid fibril formation of CPC. This work supports the universality of the amyloid-like aggregation not restricted to some special categories of protein and the fact that this aggregation can be prevented.
研究了在 0-70%(v/v)范围内逐滴加入三氟乙醇(TFE)时,鹰嘴豆半胱氨酸蛋白酶抑制剂(CPC)的构象变化和聚集体。在添加 30%和 40%(v/v)TFE 时,CPC 表现出非天然的β-折叠、内在荧光改变、硫代黄素 T 荧光增强、刚果红吸收的明显红移肩峰以及浊度和瑞利散射增强,表明形成了聚集体。TEM 结果证实了在 30%和 40%(v/v)TFE 下形成了纤维状聚集体。当 TFE 浓度增加到 70%(v/v)时,CPC 显示出保留天然样二级结构、增加的内在和 ANS 荧光。因此,我们的结果表明,CPC 纤化的有利条件在 30-40% TFE 范围内。此外,使用 ThT 结合测定法和其他生物物理测定法分析了多酚、表儿茶素(EC)和单宁酸(TA)的抗聚集作用。EC 和 TA 产生了浓度依赖性的 ThT 荧光下降,表明抑制了纤维形成。此外,与 EC 相比,TA 是 CPC 淀粉样纤维形成的更有效抑制剂。这项工作支持了淀粉样样聚集的普遍性,不受某些特殊蛋白质类别的限制,并且这种聚集可以被预防。