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球晶形成与生长的动力学:盐和蛋白质浓度对β-乳球蛋白和胰岛素的依赖性

Kinetics of spherulite formation and growth: salt and protein concentration dependence on proteins beta-lactoglobulin and insulin.

作者信息

Domike Kristin R, Donald Athene M

机构信息

Biological and Soft Systems, Cavendish Laboratory, University of Cambridge, Cambridge CB3 0HE, United Kingdom.

出版信息

Int J Biol Macromol. 2009 May 1;44(4):301-10. doi: 10.1016/j.ijbiomac.2008.12.014.

Abstract

Proteins aggregated into spherulite structures of amyloid fibrils have been observed in patients with certain brain diseases such as Alzheimer's and Parkinson's. The conditions under which these protein spherulites form and grow are not currently known. In order to illuminate the role of environmental factors on protein spherulites, this research aims to explore the kinetics and mechanisms of spherulite formation and growth, as monitored by optical microscopy, in a range of salt concentrations, and initial protein concentrations for two model proteins: bovine beta-lactoglobulin and insulin. These two proteins are significantly different in their size and fibril growth rate, but both of these proteins have been shown previously to form amyloid fibrils and spherulites under low pH conditions. The growth pattern of spherulites in each protein solution was monitored and quantified using a linear polymerisation reaction model which allowed for quantification of formation and growth rates across experiments. Two themes were found in the experimental results of spherulite formation and growth: the two model protein systems behaved very similarly to one another when viewed on relative scales, and the spherulites in these systems followed trends seen in some of the previous research of amyloid fibril growth. Specifically, in the presence of salt, both beta-lactoglobulin and insulin systems demonstrated maximum growth rates at the same salt concentration, possibly suggesting the role that salt plays in altering rates may not be protein specific (e.g. anion binding to aid unfolding), but may be generic (e.g. electrostatic shielding of repelling charges). Specifically, with variations in the initial protein concentrations, spherulite trends across both model systems were a decrease in appearance time (faster appearance) and an increased growth rate as concentration increased. The appearance time decreased at a diminishing rate towards a limiting shortest appearance time. A limiting shortest appearance time suggests that, in the higher concentrations of protein tested, spherulite formation is not dependent upon the spatial concentration of protein but on the preparedness of the protein to form or join the spherulite.

摘要

在患有某些脑部疾病(如阿尔茨海默病和帕金森病)的患者中,已观察到蛋白质聚集成淀粉样原纤维的球晶结构。目前尚不清楚这些蛋白质球晶形成和生长的条件。为了阐明环境因素对蛋白质球晶的作用,本研究旨在通过光学显微镜监测,探索两种模型蛋白(牛β-乳球蛋白和胰岛素)在一系列盐浓度和初始蛋白质浓度下球晶形成和生长的动力学及机制。这两种蛋白质在大小和原纤维生长速率上有显著差异,但先前已表明这两种蛋白质在低pH条件下都会形成淀粉样原纤维和球晶。使用线性聚合反应模型监测并量化了每种蛋白质溶液中球晶的生长模式,该模型允许对不同实验中的形成和生长速率进行量化。在球晶形成和生长的实验结果中发现了两个规律:从相对尺度来看,这两种模型蛋白质系统的行为非常相似,并且这些系统中的球晶遵循了先前一些淀粉样原纤维生长研究中观察到的趋势。具体而言,在有盐存在的情况下,β-乳球蛋白和胰岛素系统在相同盐浓度下均表现出最大生长速率,这可能表明盐在改变速率中所起的作用可能不是蛋白质特异性的(例如阴离子结合以帮助展开),而是普遍存在的(例如对排斥电荷的静电屏蔽)。具体来说,随着初始蛋白质浓度的变化,两个模型系统中球晶的趋势是出现时间减少(更快出现)且随着浓度增加生长速率增加。出现时间以逐渐减小的速率下降至极限最短出现时间。极限最短出现时间表明,在所测试的较高蛋白质浓度下,球晶的形成不依赖于蛋白质的空间浓度,而是取决于蛋白质形成或加入球晶的准备状态。

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