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追寻在颗粒细节上对 STIM1 激活进行绘图的方法。

The quest to map STIM1 activation in granular detail.

机构信息

La Jolla Institute for Immunology, La Jolla, CA 92037, USA; Moores Cancer Center, University of California-San Diego, La Jolla, CA 92037, USA; Program in Immunology, University of California-San Diego, La Jolla, CA, USA.

出版信息

Cell Calcium. 2024 Nov;123:102946. doi: 10.1016/j.ceca.2024.102946. Epub 2024 Aug 23.

Abstract

The conformational change in STIM1 that communicates sensing of ER calcium-store depletion from the STIM ER-luminal domain to the STIM cytoplasmic region and ultimately to ORAI channels in the plasma membrane is broadly understood. However, the structural basis for the STIM luminal-domain dimerization that drives the conformational change has proven elusive. A recently published study has approached this question via molecular dynamics simulations. The report pinpoints STIM residues that may be part of a luminal-domain dimerization interface, and provides unexpected insight into how torsional movements of the STIM luminal domains might trigger release of the cytoplasmic SOAR/CAD domain from its resting tethers to the STIM CC1 segments.

摘要

STIM1 构象变化将内质网钙库耗竭的感应从 STIM 内质网腔域传递到 STIM 细胞质区域,并最终传递到质膜中的 ORAI 通道,这一过程已经被广泛理解。然而,驱动构象变化的 STIM 腔域二聚化的结构基础仍难以捉摸。最近发表的一项研究通过分子动力学模拟方法探讨了这个问题。该报告确定了 STIM 残基,这些残基可能是腔域二聚化界面的一部分,并提供了意想不到的见解,说明 STIM 腔域的扭转运动如何引发细胞质 SOAR/CAD 域从其与 STIM CC1 片段的静止束缚中释放。

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