Program in Biophysical Sciences, Institute for Biophysical Dynamics, The University of Chicago, Chicago, IL, United States of America.
Department of Chemistry, The University of Chicago, Chicago, IL, United States of America.
Biochim Biophys Acta Biomembr. 2018 Oct;1860(10):2126-2133. doi: 10.1016/j.bbamem.2018.06.010. Epub 2018 Jun 18.
There is a diverse class of peripheral membrane-binding proteins that specifically bind phosphatidylserine (PS), a lipid that signals apoptosis or cell fusion depending on the membrane context of its presentation. PS-receptors are specialized for particular PS-presenting pathways, indicating that they might be sensitive to the membrane context. In this review, we describe a combination of thermodynamic, structural, and computational techniques that can be used to investigate the mechanisms underlying this sensitivity. As an example, we focus on three PS-receptors of the T-cell Immunoglobulin and Mucin containing (TIM) protein family, which we have previously shown to differ in their sensitivity to PS surface density.
有一类多样化的外周膜结合蛋白,它们特异性地结合磷脂酰丝氨酸(PS),这种脂质根据其呈现的膜环境的不同,可作为细胞凋亡或细胞融合的信号。PS 受体是专门针对特定的 PS 呈现途径的,这表明它们可能对膜环境敏感。在这篇综述中,我们描述了一组热力学、结构和计算技术的组合,可用于研究这种敏感性的潜在机制。作为一个例子,我们重点介绍了 T 细胞免疫球蛋白和粘蛋白家族(TIM)蛋白家族的三个 PS 受体,我们之前已经证明它们对 PS 表面密度的敏感性存在差异。