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独立于中心法则的生物学复制和进化的各个方面:无蛋白质囊泡转化和蛋白质介导的膜重塑的启示。

Aspects of Biological Replication and Evolution Independent of the Central Dogma: Insights from Protein-Free Vesicular Transformations and Protein-Mediated Membrane Remodeling.

机构信息

Kusuma School of Biological Sciences, Indian Institute of Technology Delhi (IIT Delhi), Hauz Khas, New Delhi, 110016, India.

Supercomputing Facility for Bioinformatics and Computational Biology (SCFBio), IIT Delhi, Hauz Khas, New Delhi, 110016, India.

出版信息

J Membr Biol. 2022 Jun;255(2-3):185-209. doi: 10.1007/s00232-022-00230-4. Epub 2022 Mar 25.

Abstract

Biological membrane remodeling is central to living systems. In spite of serving as "containers" of whole-living systems and functioning as dynamic compartments within living systems, biological membranes still find a "blue collar" treatment compared to the "white collar" nucleic acids and proteins in biology. This may be attributable to the fact that scientific literature on biological membrane remodeling is only 50 years old compared to ~ 150 years of literature on proteins and a little less than 100 years on nucleic acids. However, recently, evidence for symbiotic origins of eukaryotic cells from data only on biological membranes was reported. This, coupled with appreciation of reproducible amphiphilic self-assemblies in aqueous environments (mimicking replication), has already initiated discussions on origins of life beyond nucleic acids and proteins. This work presents a comprehensive compilation and meta-analyses of data on self-assembly and vesicular transformations in biological membranes-starting from model membranes to establishment of Influenza Hemagglutinin-mediated membrane fusion as a prototypical remodeling system to a thorough comparison between enveloped mammalian viruses and cellular vesicles. We show that viral membrane fusion proteins, in addition to obeying "stoichiometry-driven protein folding", have tighter compositional constraints on their amino acid occurrences than general-structured proteins, regardless of type/class. From the perspective of vesicular assemblies and biological membrane remodeling (with and without proteins) we find that cellular vesicles are quite different from viruses. Finally, we propose that in addition to pre-existing thermodynamic frameworks, kinetic considerations in de novo formation of metastable membrane structures with available "third-party" constituents (including proteins) were not only crucial for origins of life but also continue to offer morphological replication and/or functional mechanisms in modern life forms, independent of the central dogma.

摘要

生物膜重塑是生命系统的核心。尽管生物膜作为整个生命系统的“容器”,并在生命系统中充当动态隔室,但与生物学中的“白领”核酸和蛋白质相比,它们仍然受到“蓝领”待遇。这可能归因于这样一个事实,即与关于蛋白质的 150 多年文献相比,关于生物膜重塑的科学文献只有 50 年,而关于核酸的文献则略少于 100 年。然而,最近有证据表明,从仅关于生物膜的数据分析中,真核细胞具有共生起源。这一点,再加上对在水相环境中(模拟复制)可重复形成两亲自组装体的认识,已经引发了关于超越核酸和蛋白质的生命起源的讨论。这项工作全面汇编和分析了生物膜自组装和囊泡转化的数据——从模型膜到建立流感血凝素介导的膜融合作为典型的重塑系统,再到对包膜哺乳动物病毒和细胞囊泡的彻底比较。我们表明,病毒膜融合蛋白除了遵循“计量驱动的蛋白质折叠”外,其氨基酸出现的组成约束比一般结构蛋白更严格,无论其类型/类别如何。从囊泡组装和生物膜重塑(有蛋白和无蛋白)的角度来看,我们发现细胞囊泡与病毒有很大的不同。最后,我们提出,除了预先存在的热力学框架外,在具有可用“第三方”成分(包括蛋白质)的情况下从头形成亚稳态膜结构的动力学考虑因素不仅对生命起源至关重要,而且在现代生命形式中,独立于中心法则,继续提供形态复制和/或功能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e431/8951669/d4916e0afe03/232_2022_230_Fig1_HTML.jpg

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