Amphiphysin的n端两亲螺旋可以改变RBL-2H3肥大细胞突触中免疫球蛋白E受体(FcεRI)的空间分布

Kathrin Spendier
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引用次数: 3

摘要

当生物膜执行重要的细胞功能或患病时,它们会经历广泛的形状变化。为了了解脂质和蛋白质在不同过程中控制膜曲率的机制,研究人员已经确定并设计了许多曲率诱导和曲率传感的蛋白质和肽。本文通过一个简单的实验定性地展示了Amphiphysin n端两亲螺旋的膜重塑如何影响肥大细胞中跨膜Fc受体蛋白(Fcε ri)的空间分布。结果表明,两亲螺旋浓度升高会干扰典型肥大细胞突触的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
N-terminal amphipathic helix of Amphiphysin can change the spatial distribution of immunoglobulin E receptors (FcεRI) in the RBL-2H3 mast cell synapse

Biomembranes undergo extensive shape changes as they perform vital cellular functions or become diseased. To understand the mechanisms by which lipids and proteins control membrane curvature during various processes, researchers have identified and engineered many curvature-inducing and curvature-sensing proteins and peptides. In this paper, a simple experiment was performed to show qualitatively how membrane remodeling by N-terminal amphipathic helix of Amphiphysin affects the spatial distribution of the transmembrane Fc receptor protein (FcεRI) in mast cells. Results indicate that an elevated concentration of amphipathic helices can interfere with the formation of a typical mast cell synapse.

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