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跨学科协同揭示膜联蛋白介导的质膜重塑和修复的机制。

Interdisciplinary Synergy to Reveal Mechanisms of Annexin-Mediated Plasma Membrane Shaping and Repair.

机构信息

Niels Bohr Institute, University of Copenhagen, DK-2100 Copenhagen, Denmark.

Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, DK-5230 Odense, Denmark.

出版信息

Cells. 2020 Apr 21;9(4):1029. doi: 10.3390/cells9041029.

Abstract

The plasma membrane surrounds every single cell and essentially shapes cell life by separating the interior from the external environment. Thus, maintenance of cell membrane integrity is essential to prevent death caused by disruption of the plasma membrane. To counteract plasma membrane injuries, eukaryotic cells have developed efficient repair tools that depend on Ca- and phospholipid-binding annexin proteins. Upon membrane damage, annexin family members are activated by a Ca influx, enabling them to quickly bind at the damaged membrane and facilitate wound healing. Our recent studies, based on interdisciplinary research synergy across molecular cell biology, experimental membrane physics, and computational simulations show that annexins have additional biophysical functions in the repair response besides enabling membrane fusion. Annexins possess different membrane-shaping properties, allowing for a tailored response that involves rapid bending, constriction, and fusion of membrane edges for resealing. Moreover, some annexins have high affinity for highly curved membranes that appear at free edges near rupture sites, a property that might accelerate their recruitment for rapid repair. Here, we discuss the mechanisms of annexin-mediated membrane shaping and curvature sensing in the light of our interdisciplinary approach to study plasma membrane repair.

摘要

细胞膜包围着每一个细胞,通过将内部与外部环境分隔开来,从本质上塑造了细胞的生命。因此,保持细胞膜的完整性对于防止因细胞膜破裂而导致的细胞死亡至关重要。为了对抗细胞膜损伤,真核细胞已经开发出了有效的修复工具,这些工具依赖于 Ca 和磷脂结合的膜联蛋白。在膜损伤时,膜联蛋白家族成员通过 Ca2+内流被激活,使它们能够迅速结合在受损的膜上,并促进伤口愈合。我们最近的研究基于分子细胞生物学、实验膜物理学和计算模拟的跨学科研究协同作用,表明膜联蛋白在修复反应中除了能够促进膜融合之外,还具有其他生物物理功能。膜联蛋白具有不同的膜成形特性,允许进行定制化的响应,包括快速弯曲、收缩和膜边缘融合以进行重新密封。此外,一些膜联蛋白对在破裂部位附近的自由边缘出现的高度弯曲的膜具有高亲和力,这种特性可能会加速它们的募集,以实现快速修复。在这里,我们根据我们的跨学科方法来研究细胞膜修复,讨论了膜联蛋白介导的膜成形和曲率感应的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ac/7226303/c7911b10ff4b/cells-09-01029-g001.jpg

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