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DNA 介导的肽组装成蛋白质模拟物。

DNA-Mediated Peptide Assembly into Protein Mimics.

机构信息

Department of Chemistry, McGill University, 801 Sherbrooke St. W., Montreal, QC H3A0B8, Canada.

Department of Chemistry and Interdisciplinary Nanoscience Centre (iNANO), Aarhus University, Gustav Wieds Vej 14, Aarhus C, Aarhus 8000, Denmark.

出版信息

J Am Chem Soc. 2024 Jan 24;146(3):1946-1956. doi: 10.1021/jacs.3c08984. Epub 2024 Jan 16.

Abstract

The design of new protein structures is challenging due to their vast sequence space and the complexity of protein folding. Here, we report a new modular DNA-templated strategy to construct protein mimics. We achieve the spatial control of multiple peptide units by conjugation with DNA and hybridization to a branched DNA trimer template followed by covalent stapling of the preorganized peptides into a single unit. A library of protein mimics with different lengths, sequences, and heptad registers has been efficiently constructed. DNA-templated protein mimics show an α-helix or coiled-coil motif formation even when they are constructed from weakly interacting peptide units. Their attached DNA handles can be used to exert dynamic control over the protein mimics' secondary and tertiary structures. This modular strategy will facilitate the development of DNA-encoded protein libraries for the rapid discovery of new therapeutics, enzymes, and antibody mimics.

摘要

由于蛋白质结构的序列空间非常庞大,以及蛋白质折叠的复杂性,设计新的蛋白质结构极具挑战性。在这里,我们报告了一种新的模块化 DNA 模板策略,用于构建蛋白质模拟物。我们通过与 DNA 缀合并与分支 DNA 三聚体模板杂交来实现多个肽单位的空间控制,然后将预组织的肽共价键合到单个单元中。已经高效构建了具有不同长度、序列和七肽寄存器的蛋白质模拟物文库。即使使用弱相互作用的肽单元构建,DNA 模板化的蛋白质模拟物也能形成 α-螺旋或卷曲螺旋结构。它们连接的 DNA 接头可用于对蛋白质模拟物的二级和三级结构进行动态控制。这种模块化策略将促进 DNA 编码的蛋白质文库的发展,从而快速发现新的治疗药物、酶和抗体模拟物。

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