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超越流动性的膜动态平衡:膜可压缩性的控制。

Membrane homeostasis beyond fluidity: control of membrane compressibility.

机构信息

Medical Biochemistry and Molecular Biology, Medical Faculty, Saarland University, Homburg, Germany; PZMS, Center for Molecular Signaling, Medical Faculty, Saarland University, Homburg, Germany.

出版信息

Trends Biochem Sci. 2023 Nov;48(11):963-977. doi: 10.1016/j.tibs.2023.08.004. Epub 2023 Aug 29.

Abstract

Biomembranes are complex materials composed of lipids and proteins that compartmentalize biochemistry. They are actively remodeled in response to physical and metabolic cues, as well as during cell differentiation and stress. The concept of homeoviscous adaptation has become a textbook example of membrane responsiveness. Here, we discuss limitations and common misconceptions revolving around it. By highlighting key moments in the life cycle of a transmembrane protein, we illustrate that membrane thickness and a finely regulated membrane compressibility are crucial to facilitate proper membrane protein insertion, function, sorting, and inheritance. We propose that the unfolded protein response (UPR) provides a mechanism for endoplasmic reticulum (ER) membrane homeostasis by sensing aberrant transverse membrane stiffening and triggering adaptive responses that re-establish membrane compressibility.

摘要

生物膜是由脂质和蛋白质组成的复杂材料,它们将生物化学分隔开来。生物膜会根据物理和代谢线索以及细胞分化和应激做出积极的重塑。同源粘弹性适应的概念已成为膜响应性的教科书范例。在这里,我们讨论了围绕它的局限性和常见误解。通过突出跨膜蛋白生命周期中的关键时刻,我们说明膜厚度和精细调节的膜压缩性对于促进适当的膜蛋白插入、功能、分类和遗传至关重要。我们提出,未折叠蛋白反应 (UPR) 通过感测异常的横向膜硬度并触发恢复膜压缩性的适应性反应,为内质网 (ER) 膜的动态平衡提供了一种机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/459e/10580326/f75a64b18028/gr1.jpg

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