质膜的不对称性和非均质性。

IF 3.2 3区 生物学 Q2 BIOPHYSICS
Teppei Yamada, Wataru Shinoda
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引用次数: 0

摘要

质膜(PMs)在磷脂头基团、不饱和以及由此产生的膜特性(如填料和流动性)方面表现出两个小叶之间的不对称性。侧异质性,包括脂质结构域的形成,是pm的另一个重要方面,具有重要的生物学意义。然而,在PMs的两个小叶中脂质结构域的性质甚至存在仍然难以捉摸,阻碍了对脂质不对称意义的完整理解。通过粗粒度分子动力学模拟,我们发现不对称PM的外层小叶脂质高度有序且分布均匀,而内部小叶分离成纳米尺度(≈10 nm)的高度有序和更无序的结构域,表现出高度动态的结构域融合和裂变事件。由于胆固醇偏向外侧小叶,这种结构的不对称进一步加强。这些发现表明两个小叶的不同功能作用,由不对称侧应力调节。此外,比较不对称和完全打乱的PM的相行为揭示了结构域大小的关键决定因素:完整的PM保持纳米级结构域,而细胞来源的巨大PM囊泡失去了严格的脂质不对称,呈现微尺度结构域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Asymmetry and heterogeneity in the plasma membrane.

Plasma membranes (PMs) exhibit asymmetry between their two leaflets in terms of phospholipid headgroups, unsaturation, and resulting membrane properties, such as packing and fluidity. Lateral heterogeneity, including the formation of lipid domains, is another crucial aspect of PMs with significant biological implications. However, the nature and even the existence of lipid domains in the two leaflets of PMs remain elusive, hindering a complete understanding of the significance of lipid asymmetry. Using coarse-grained molecular dynamics simulations of the asymmetric PM, we find that the outer leaflet lipids are highly ordered and largely uniformly distributed, whereas the inner leaflet separates into nanoscale (≈10 nm) highly ordered and more disordered domains, exhibiting highly dynamic domain fusion and fission events. This structural asymmetry is further reinforced by asymmetric lateral stress resulting from a cholesterol bias toward the outer leaflet. These findings suggest distinct functional roles for the two leaflets modulated by asymmetric lateral stress. Additionally, comparing the phase behavior of asymmetric and fully scrambled PMs reveals a key determinant of domain size: intact PMs maintain nanoscale domains, whereas cell-derived giant PM vesicles, which have lost the strict lipid asymmetry, exhibit microscale domains.

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来源期刊
Biophysical journal
Biophysical journal 生物-生物物理
CiteScore
6.10
自引率
5.90%
发文量
3090
审稿时长
2 months
期刊介绍: BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.
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