串联结蛋白的折叠:多肽链可以脱离深层动力学陷阱的证据。

IF 4.5 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Protein Science Pub Date : 2025-03-01 DOI:10.1002/pro.70048
Hongyu Zhang, Sophie E Jackson
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引用次数: 0

摘要

很难想象蛋白质是如何在多肽链上打结的,但事实确实如此。这些复杂的拓扑结构挑战了传统的简单漏斗状能量景观的蛋白质折叠观点。先前对具有单个三叶结的深结蛋白质折叠机制的实验研究已经证明,这种拓扑结构比其他简单蛋白质具有更复杂的折叠景观。然而,到目前为止,还没有尝试研究任何蛋白质的折叠,其中需要多个线程事件在单个多肽链中产生多个结。在这里,我们报告了人工串联结蛋白的构建和表征。我们发现令人信服的证据,这两个区域的蛋白质形成三叶结具有相似的结构和稳定性的亲本单一三叶结蛋白。此外,我们表明这种串联结蛋白具有复杂的折叠途径,其中有额外的非常缓慢的折叠阶段,我们提出对应于系统内第二个结的形成。我们还发现证据表明,在折叠过程中,这种蛋白质被短暂地困在深层的动力学陷阱中,然而,大多数蛋白质链(>90%)设法部分展开并获得天然的串联结拓扑结构。这项工作强调了这样一个事实,即大自然可以容忍比我们想象的更复杂的蛋白质拓扑结构,尽管在折叠过程中存在相当大的错误折叠,蛋白质链即使在没有分子伴侣的情况下也能找到通往天然状态的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Folding of a tandemly knotted protein: Evidence that a polypeptide chain can get out of deep kinetic traps.

It is hard to imagine how proteins can thread and form knots in their polypeptide chains, but they do. These topologically complex structures have challenged the traditional protein folding views of simple funnel-shaped energy landscapes. Previous experimental studies on the folding mechanisms of deeply knotted proteins with a single trefoil knot have yielded evidence that this topology has a more complicated folding landscape than other simpler proteins. However, to date, there have been no attempts to study the folding of any protein in which multiple threading events are needed to create more than one knot within a single polypeptide chain. Here, we report the construction and characterization of an artificial tandemly knotted protein. We find compelling evidence that both domains of the protein form trefoil knots with similar structures and stabilities to the parent single trefoil-knotted protein. In addition, we show that this tandemly knotted protein has a complex folding pathway in which there are additional very slow folding phases that we propose correspond to the formation of the second knot within the system. We also find evidence that during folding this protein gets transiently trapped in deep kinetic traps, however, the majority of protein chains (>90%) manage to partially unfold and acquire the native tandem-knot topology. This work highlights the fact that Nature can tolerate more complex protein topologies than we thought, and despite considerable misfolding during folding, protein chains can find their way to the native state even in the absence of molecular chaperones.

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来源期刊
Protein Science
Protein Science 生物-生化与分子生物学
CiteScore
12.40
自引率
1.20%
发文量
246
审稿时长
1 months
期刊介绍: Protein Science, the flagship journal of The Protein Society, is a publication that focuses on advancing fundamental knowledge in the field of protein molecules. The journal welcomes original reports and review articles that contribute to our understanding of protein function, structure, folding, design, and evolution. Additionally, Protein Science encourages papers that explore the applications of protein science in various areas such as therapeutics, protein-based biomaterials, bionanotechnology, synthetic biology, and bioelectronics. The journal accepts manuscript submissions in any suitable format for review, with the requirement of converting the manuscript to journal-style format only upon acceptance for publication. Protein Science is indexed and abstracted in numerous databases, including the Agricultural & Environmental Science Database (ProQuest), Biological Science Database (ProQuest), CAS: Chemical Abstracts Service (ACS), Embase (Elsevier), Health & Medical Collection (ProQuest), Health Research Premium Collection (ProQuest), Materials Science & Engineering Database (ProQuest), MEDLINE/PubMed (NLM), Natural Science Collection (ProQuest), and SciTech Premium Collection (ProQuest).
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