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Structural Basis for C2'-methoxy Recognition by DNA Polymerases and Function Improvement.
Wen, Chongzheng; Wang, Guangyuan; Yang, Lin; Chen, Tingjian; Liu, Haiping; Gong, Weimin.
Afiliação
  • Wen C; Division of Biological Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230027, PR China.
  • Wang G; MOE International Joint Research Laboratory on Synthetic Biology and Medicines, School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, PR China.
  • Yang L; Division of Biological Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230027, PR China.
  • Chen T; MOE International Joint Research Laboratory on Synthetic Biology and Medicines, School of Biology and Biological Engineering, South China University of Technology, Guangzhou 510006, PR China. Electronic address: chentj@scut.edu.cn.
  • Liu H; Division of Biological Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230027, PR China. Electronic address: haipingliu@ustc.edu.cn.
  • Gong W; Division of Biological Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230027, PR China. Electronic address: wgong@ustc.edu.cn.
J Mol Biol ; 436(20): 168744, 2024 Oct 15.
Article em En | MEDLINE | ID: mdl-39147125
ABSTRACT
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Modelos Moleculares Idioma: En Revista: J Mol Biol Ano de publicação: 2024 Tipo de documento: Article País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Modelos Moleculares Idioma: En Revista: J Mol Biol Ano de publicação: 2024 Tipo de documento: Article País de publicação: Holanda