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阿斯加德古菌中真核生物脂质转移蛋白折叠的起源。

An origin for a eukaryotic lipid transfer protein fold in Asgard archaea.

作者信息

Lipp Nicolas-Frédéric, Budin Itay

机构信息

Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA 92093, USA.

出版信息

bioRxiv. 2025 Jun 8:2025.05.16.653879. doi: 10.1101/2025.05.16.653879.

Abstract

The evolution of eukaryotic cells necessitated the advent of machinery to transport molecular building blocks for organelles to proliferate. Extant eukaryotes share several classes of highly conserved lipid transfer proteins (LTP) that associate with donor membranes, bind individual lipid molecules, and shuttle them to acceptor membranes. Because cells lacking organelles do not require extensive lipid transport networks, it is not known if this machinery pre-dated eukaryotic organelles or had to evolve alongside them. Here we describe a class of putative lipid transporters in the Asgard archaeota superphylum that share a common ancestry with eukaryotic LTPs in the START domain superfamily. We identified three classes of Asgard START proteins, StarAsg1-3, which are conserved across most Asgard phyla. Of these, StarAsg1 family proteins contain the predicted structural features necessary for lipid transfer: large, hydrophobic binding pockets lined with amphipathic motifs for membrane docking. In contrast, StarAsg2 and StarAsg3 family proteins contain smaller binding cavities and minimal predicted membrane interactions. We found that StarAsg1 from Lokiarcheota interacts with anionic membranes both in vitro and in yeast cells and can transfer sterols between liposomes. Phylogenetic analysis of START domains across the tree of life indicates that eukaryotic LTPs share a common ancestry with StarAsg1 homologs, while StarAsg2 and StarAsg3 form a monophyletic group with eukaryotic heat shock protein cochaperones. We propose that the emergence of proteins for inter-membrane lipid transporters in the ancestors of eukaryotic cells could have facilitated the subsequent development of intracellular organelles.

摘要

真核细胞的进化需要出现用于运输细胞器分子构件以实现增殖的机制。现存的真核生物共享几类高度保守的脂质转移蛋白(LTP),这些蛋白与供体膜结合,结合单个脂质分子,并将它们穿梭到受体膜。由于缺乏细胞器的细胞不需要广泛的脂质运输网络,因此尚不清楚这种机制是早于真核细胞器出现,还是必须与它们一起进化。在这里,我们描述了阿斯加德古菌超门中的一类假定脂质转运蛋白,它们与START结构域超家族中的真核LTP有着共同的祖先。我们鉴定出三类阿斯加德START蛋白,即StarAsg1 - 3,它们在大多数阿斯加德门类中都很保守。其中,StarAsg1家族蛋白包含脂质转移所需的预测结构特征:大型疏水结合口袋,内衬两亲性基序用于膜对接。相比之下,StarAsg2和StarAsg3家族蛋白包含较小的结合腔和最少的预测膜相互作用。我们发现来自洛基古菌的StarAsg1在体外和酵母细胞中都能与阴离子膜相互作用,并能在脂质体之间转移固醇。对生命之树中START结构域的系统发育分析表明,真核LTP与StarAsg1同源物有着共同的祖先,而StarAsg2和StarAsg3与真核热休克蛋白伴侣形成一个单系群。我们提出,真核细胞祖先中用于膜间脂质转运蛋白的出现可能促进了细胞内细胞器的后续发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f73/12147543/20959cff9b46/nihpp-2025.05.16.653879v2-f0001.jpg

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