Bacteriophage protein Gp46 is a cross-species inhibitor of nucleoid-associated HU proteins

Author:

Zhang Peipei12ORCID,Zhao Xiaohui3,Wang Yawen12,Du Ke12,Wang Zhihao24,Yu Jianfeng4ORCID,Chang Gang5ORCID,Matthews Steve4ORCID,Wang Hongliang3ORCID,Liu Bing125ORCID

Affiliation:

1. Department of Laboratory Medicine, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China

2. BioBank, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China

3. Department of Pathogen Biology and Immunology, Xi'an Jiaotong University Health Science Center, Xi'an 710061, China

4. Department of Life Sciences, Imperial College London, SW7 2AZ London, United Kingdom

5. Instrument Analysis Center of Xi'an, Jiaotong University, Xi'an 710049, China

Abstract

Significance Histone-like protein from Escherichia coli strain U93 (HU) protein is the most abundant nucleoid-associated protein in bacteria, which plays a fundamental role in chromosomal compaction and organization. It is essential for most bacteria as well as Apicomplexans, thus an important target for the development of antimicrobial and antimalaria drugs. We report Gp46 as a phage protein HU inhibitor. It inhibits HU of Bacillus subtilis by occupying its DNA binding site, thus preventing chromosome segregation during cell division. As key residues for the interaction are highly conserved, Gp46 interacts with HUs of a broad range of pathogens, including many pathogenic bacteria and Apicomplexan parasites like Plasmodium falciparum. Thus, this cross-species property could benefit antibiotic and antimalaria drug development that targets HU.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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