Exploring the mechanism how AF9 recognizes and binds H3K9ac by molecular dynamics simulations and free energy calculations

• Published in: Biopolymers 2016-11, Vol.105 (11), p.779-786
• Main Authors: Wang, Quan, Zheng, Qing‐Chuan, Zhang, Hong‐Xing
• Format: Article
• Language: English
• Subjects: Acetylation; H3K9ac peptides; histone lysine acetylation; Histones; Histones - chemistry; Histones - metabolism; Humans; hydrophobic surface; Lysine; MM/PBSA; Molecular dynamics; Molecular Dynamics Simulation; Nuclear Proteins - chemistry; Nuclear Proteins - metabolism; Peptides; Protein Binding; Proteins; Recognition; Simulation
• ISSN: 0006-3525; 1097-0282
• DOI: 10.1002/bip.22896

ABSTRACT Histone acetylation is a very important regulatory mechanism in gene expression in the chromatin context. A new protein family‐YEATS domains have been found as a novel histone acetylation reader, which could specific recognize the histone lysine acetylation. AF9 is an important one in the YEATS family. Focused on the AF9‐H3K9ac (K9 acetylation) complex (ALY) (PDB code: 4TMP) and a serials of mutants, MUT (the acetyllsine of H3K9ac was mutated to lysine), F59A, G77A, and D103A, we applied molecular dynamics simulation and molecular mechanics Poisson−Boltzmann (MM‐PBSA) free energy calculations to examine the role of AF9 protein in recognition interaction. The simulation results and analysis indicate that some residues of the protein have significant influence on recognition and binding to H3K9ac peptides and hydrophobic surface show the hydrophobic interactions play an important role in the binding. Our work can give important information to understand how the protein AF9 recognizes the peptides H3K9ac. © 2016 Wiley Periodicals, Inc. Biopolymers 105: 779–786, 2016.