Structural basis and affinity improvement for an ATP-binding

• 成果类型: Article
• 署名作者: Jiang, Yan; Zhang, Yuchao; Wan, Liqi; Cui, Cheng; Guo, Pei; Han, Da; Tan, Weihong; Patel, Dinshaw
• 署名单位: Hunan University; Chinese Academy of Sciences; Hangzhou Institute of Medicine, CAS; Shanghai Jiao Tong University
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-14743
• DOI: 10.1073/pnas.2506491122
• 发表日期: 2025-08-14
• 关键词: magnesium-ions; dna aptamer; rna; RECOGNITION; adenosine

摘要

DNA aptamers that bind small molecules with high affinity have revolutionized the fields of biosensing and bioimaging. Recently, a DNA aptamer named 1301b has been identified as the most potent DNA aptamer for the binding of adenosine triphosphate (ATP) with a dissociation constant (K-D) of similar to 2.7 mu M. However, the structural basis and recognition mechanism remain unclear, hindering further development of this DNA aptamer. In this study, we first design a shortened DNA aptamer namely 1301b_v1 that retains a good affinity for ATP and then determine the tertiary structure of 1:1 1301b_v1-ATP binding complex using solution NMR spectroscopy. The overall complex structure shows an L shape architecture with the binding pocket formed by two internal loops. The ATP intercalates into the binding pocket through forming hydrogen bond with G14 and stacking with T8 center dot A28 and G9. We also reveal an adaptive binding mechanism where the DNA aptamer switches from a semifolded state to a stable tertiary structure upon ATP binding. Based on the structure-function relationship, we introduce 2 '-O-methyl modification to residues in the central junction and obtain a DNA aptamer named 9/10/16(OMe) with a KD of similar to 0.7 mu M for the binding of ATP. These results underscore the ability of DNA molecules to form intricate three-dimensional folds with sophisticated functionality, opening up avenues for designing novel DNA-based molecular tools.