Structural and Biochemical Basis for Development of Influenza Virus Inhibitors Targeting the PA Endonuclease

PLoS Pathogens

Mi-Kyung Yun¹  Brandi M. Baughman¹  P. Jake Slavish²  Stephen W. White²  Rebecca M. DuBois³  Richard J. Webby³  Thomas R. Webb³  Ju Bao⁴ 

[1] Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America;Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America;Department of Structural Biology, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America;Integrated Program in Biomedical Sciences, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America

关键词: Crystal structure;    Oxygen;    Influenza viruses;    Manganese;    Influenza A virus;    Electron density;    Sequence alignment;    Crystals;   

DOI  :  10.1371/journal.ppat.1002830

学科分类：生物科学（综合）

来源: Public Library of Science

【 摘 要 】

Emerging influenza viruses are a serious threat to human health because of their pandemic potential. A promising target for the development of novel anti-influenza therapeutics is the PA protein, whose endonuclease activity is essential for viral replication. Translation of viral mRNAs by the host ribosome requires mRNA capping for recognition and binding, and the necessary mRNA caps are cleaved or “snatched” from host pre-mRNAs by the PA endonuclease. The structure-based development of inhibitors that target PA endonuclease is now possible with the recent crystal structure of the PA catalytic domain. In this study, we sought to understand the molecular mechanism of inhibition by several compounds that are known or predicted to block endonuclease-dependent polymerase activity. Using an in vitro endonuclease activity assay, we show that these compounds block the enzymatic activity of the isolated PA endonuclease domain. Using X-ray crystallography, we show how these inhibitors coordinate the two-metal endonuclease active site and engage the active site residues. Two structures also reveal an induced-fit mode of inhibitor binding. The structures allow a molecular understanding of the structure-activity relationship of several known influenza inhibitors and the mechanism of drug resistance by a PA mutation. Taken together, our data reveal new strategies for structure-based design and optimization of PA endonuclease inhibitors.

【 授权许可】

CC BY