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折叠中的折叠:探索单一结构域蛋白的拓扑异构体。

Folds from fold: Exploring topological isoforms of a single-domain protein.

机构信息

Beijing National Laboratory for Molecular Sciences, Department of Polymer Science and Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, People's Republic of China.

Key Laboratory of Polymer Chemistry & Physics of Ministry of Education, Center for Soft Matter Science and Engineering, Peking University, Beijing 100871, People's Republic of China.

出版信息

Proc Natl Acad Sci U S A. 2024 Oct 22;121(43):e2407355121. doi: 10.1073/pnas.2407355121. Epub 2024 Oct 15.

Abstract

Expanding the protein fold space beyond linear chains is of fundamental significance, yet remains largely unexplored. Herein, we report the creation of seven topological isoforms (i.e., linear, cyclic, knot, lasso, pseudorotaxane, and catenane) from a single protein fold precursor by rewiring the connectivity of secondary structure elements of the SpyTag-SpyCatcher complex and mutating the reactive residue on SpyTag to abolish the isopeptide bonding. These topological isoforms can be directly expressed in cells. Their topologies were confirmed by combined techniques of proteolytic digestion, fluorescence correlation spectroscopy (FCS), size-exclusion chromatography (SEC), and topological transformation. To study the effects of topology on their structures and properties, their biophysical properties were characterized by differential scanning calorimetry (DSC), heteronuclear single quantum coherence nuclear magnetic resonance spectroscopy (HSQC-NMR), and circular dichroism (CD) spectroscopy. Molecular dynamics (MD) simulations were further performed to reveal the atomic details of structural changes upon unfolding. Both experimental and simulation results suggest that they share a similar, well-folded hydrophobic core but exhibit distinct folding/unfolding dynamic behaviors. These results shed light onto the folding landscape of topological isoforms derived from the same protein fold. As a model system, this work improves our understanding of protein structure and dynamics beyond linear chains and suggests that protein folds are highly amenable to topological variation.

摘要

拓展线性链以外的蛋白质折叠空间具有重要意义,但目前仍在很大程度上尚未得到探索。在此,我们通过重新连接 SpyTag-SpyCatcher 复合物的二级结构元件的连接性,并突变 SpyTag 上的反应性残基以消除异肽键,从单个蛋白质折叠前体中创建了七种拓扑异构体(即线性、环状、纽结、套索、假轮烷和索烃)。这些拓扑异构体可以直接在细胞中表达。通过酶解、荧光相关光谱(FCS)、尺寸排阻色谱(SEC)和拓扑转化相结合的技术,证实了它们的拓扑结构。为了研究拓扑结构对它们结构和性能的影响,通过差示扫描量热法(DSC)、异核单量子相干核磁共振波谱(HSQC-NMR)和圆二色性(CD)光谱对它们的生物物理性质进行了表征。进一步进行分子动力学(MD)模拟以揭示解折叠过程中结构变化的原子细节。实验和模拟结果均表明,它们具有相似的、折叠良好的疏水性核心,但表现出不同的折叠/去折叠动态行为。这些结果揭示了源自相同蛋白质折叠的拓扑异构体的折叠景观。作为一个模型系统,这项工作提高了我们对线性链以外的蛋白质结构和动力学的理解,并表明蛋白质折叠非常适合拓扑变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/609d/11513978/8d623dded45f/pnas.2407355121fig01.jpg

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