{"title":"DNA 聚合酶识别 C2'-methoxy 的结构基础和功能改进。","authors":"","doi":"10.1016/j.jmb.2024.168744","DOIUrl":null,"url":null,"abstract":"<div><p>DNA modified with C2′-methoxy (C2′-OMe) greatly enhances its resistance to nucleases, which is beneficial for the half-life of aptamers and DNA nanomaterials. Although the unnatural DNA polymerases capable of incorporating C2′-OMe modified nucleoside monophosphates (C2′-OMe-NMPs) were engineered via directed evolution, the detailed molecular mechanism by which an evolved DNA polymerase recognizes C2′-OMe-NTPs remains poorly understood. Here, we present the crystal structures of the evolved Stoffel fragment of Taq DNA polymerase SFM4-3 processing the C2′-OMe-GTP in different states. Our results reveal the structural basis for recognition of C2′-methoxy by SFM4-3. Based on the analysis of other mutated residues in SFM4-3, a new Stoffel fragment variant with faster catalytic rate and stronger inhibitor-resistance was obtained. In addition, the capture of a novel pre-insertion co-existing with template 5′-overhang stacking conformation provides insight into the catalytic mechanism of Taq DNA polymerase.</p></div>","PeriodicalId":369,"journal":{"name":"Journal of Molecular Biology","volume":null,"pages":null},"PeriodicalIF":4.7000,"publicationDate":"2024-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Structural Basis for C2′-methoxy Recognition by DNA Polymerases and Function Improvement\",\"authors\":\"\",\"doi\":\"10.1016/j.jmb.2024.168744\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>DNA modified with C2′-methoxy (C2′-OMe) greatly enhances its resistance to nucleases, which is beneficial for the half-life of aptamers and DNA nanomaterials. Although the unnatural DNA polymerases capable of incorporating C2′-OMe modified nucleoside monophosphates (C2′-OMe-NMPs) were engineered via directed evolution, the detailed molecular mechanism by which an evolved DNA polymerase recognizes C2′-OMe-NTPs remains poorly understood. Here, we present the crystal structures of the evolved Stoffel fragment of Taq DNA polymerase SFM4-3 processing the C2′-OMe-GTP in different states. Our results reveal the structural basis for recognition of C2′-methoxy by SFM4-3. Based on the analysis of other mutated residues in SFM4-3, a new Stoffel fragment variant with faster catalytic rate and stronger inhibitor-resistance was obtained. In addition, the capture of a novel pre-insertion co-existing with template 5′-overhang stacking conformation provides insight into the catalytic mechanism of Taq DNA polymerase.</p></div>\",\"PeriodicalId\":369,\"journal\":{\"name\":\"Journal of Molecular Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-08-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Molecular Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S002228362400353X\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S002228362400353X","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
用C2'-甲氧基(C2'-OMe)修饰的DNA可大大增强其对核酸酶的抗性,这有利于提高适配体和DNA纳米材料的半衰期。虽然通过定向进化设计出了能够结合 C2'-OMe 修饰的单磷酸核苷(C2'-OMe-NMPs)的非天然 DNA 聚合酶,但人们对进化 DNA 聚合酶识别 C2'-OMe-NTPs 的详细分子机制仍然知之甚少。在这里,我们展示了进化的 Taq DNA 聚合酶 SFM4-3 的 Stoffel 片段在不同状态下处理 C2'-OMe-GTP 的晶体结构。我们的研究结果揭示了 SFM4-3 识别 C2'-methoxy 的结构基础。基于对 SFM4-3 中其他突变残基的分析,我们得到了一个新的斯托弗片段变体,它具有更快的催化速率和更强的抗抑制剂能力。此外,捕获到的一种新型预插入与模板 5'-overhang 堆积构象共存的现象也为 Taq DNA 聚合酶的催化机理提供了启示。
Structural Basis for C2′-methoxy Recognition by DNA Polymerases and Function Improvement
DNA modified with C2′-methoxy (C2′-OMe) greatly enhances its resistance to nucleases, which is beneficial for the half-life of aptamers and DNA nanomaterials. Although the unnatural DNA polymerases capable of incorporating C2′-OMe modified nucleoside monophosphates (C2′-OMe-NMPs) were engineered via directed evolution, the detailed molecular mechanism by which an evolved DNA polymerase recognizes C2′-OMe-NTPs remains poorly understood. Here, we present the crystal structures of the evolved Stoffel fragment of Taq DNA polymerase SFM4-3 processing the C2′-OMe-GTP in different states. Our results reveal the structural basis for recognition of C2′-methoxy by SFM4-3. Based on the analysis of other mutated residues in SFM4-3, a new Stoffel fragment variant with faster catalytic rate and stronger inhibitor-resistance was obtained. In addition, the capture of a novel pre-insertion co-existing with template 5′-overhang stacking conformation provides insight into the catalytic mechanism of Taq DNA polymerase.
期刊介绍:
Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions.
Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.