New insights into protein–DNA binding specificity from hydrogen bond based comparative study

• Published in: Nucleic acids research Vol. 47; no. 21; pp. 11103 - 11113
• Main Authors: Lin, Maoxuan, Guo, Jun-tao
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 02-12-2019
• Subjects: Amino Acids - chemistry; Base Pairing; Binding Sites; Computational Biology; DNA - chemistry; DNA-Binding Proteins - chemistry; Hydrogen Bonding; Models, Molecular; Nucleic Acid Conformation; Protein Structure, Secondary
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gkz963

Abstract
Knowledge of protein–DNA binding specificity has important implications in understanding DNA metabolism, transcriptional regulation and developing therapeutic drugs. Previous studies demonstrated hydrogen bonds between amino acid side chains and DNA bases play major roles in specific protein–DNA interactions. In this paper, we investigated the roles of individual DNA strands and protein secondary structure types in specific protein–DNA recognition based on side chain-base hydrogen bonds. By comparing the contribution of each DNA strand to the overall binding specificity between DNA-binding proteins with different degrees of binding specificity, we found that highly specific DNA-binding proteins show balanced hydrogen bonding with each of the two DNA strands while multi-specific DNA binding proteins are generally biased towards one strand. Protein-base pair hydrogen bonds, in which both bases of a base pair are involved in forming hydrogen bonds with amino acid side chains, are more prevalent in the highly specific protein–DNA complexes than those in the multi-specific group. Amino acids involved in side chain-base hydrogen bonds favor strand and coil secondary structure types in highly specific DNA-binding proteins while multi-specific DNA-binding proteins prefer helices.