Characterization of amino acid residues essential for tetramer formation and DNA-binding activity of ssDNA-binding protein of Mycobacterium tuberculosis.

Abstract

Mycobacterium tuberculosis Rv0054 encodes a single-stranded DNA-binding protein (MtbSSB) that is essential for survival of the human pathogen and causative agent of tuberculosis. The function of MtbSSB has been proposed to be different from its E. coli homolog. However, the critical amino acid residues of MtbSSB and their regulatory effects on DNA-binding ability remain to be clearly characterized. In this study, using a frequency-controlled random mutagenesis method (FRM), mutant libraries of MtbSSB were successfully constructed. On the whole, 146 single, double, and triple MtbSSB mutants, which covered 89% of the amino acid residues along the whole MtbSSB gene, were isolated. Using bacterial two-hybrid assays in combination with native PAGE assays, four new mutants, E62G, D104N, E94G/T137N, and S130P/G153N were found to totally or partially lose their ability to form tetramer. Three novel mutants, E62G, D104N, and E94G/T134N, were characterized to have a much lower ssDNA-binding activity, while one mutant, F21L, was found to have a significantly higher activity through both electrophoretic mobility shift and surface plasmon resonance assays. Interestingly, three amino acid residues, E62, D104, and E94, were found to regulate both oligomerization and ssDNA-binding activity of MtbSSB. Our work provides an important resource and should help improve the understanding of the biochemical mechanisms and structure-function relationship of the DNA-binding protein in this important human pathogen.

• Authors: Hua Zhang, Yuxi Tian, Ziduo Liu, Feng Huang, Lihua Hu, Zheng-Guo He
• Journal: Biochemistry. Biokhimiia (Biochemistry (Mosc)) Vol. 76 Issue 6 Pg. 658-65 (Jun 2011) ISSN: 1608-3040 [Electronic] United States
• PMID: 21639846 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Bacterial Proteins
• DNA, Single-Stranded
• DNA-Binding Proteins

Topics

• Amino Acid Substitution
• Bacterial Proteins (chemistry, genetics, metabolism)
• DNA, Single-Stranded (chemistry, metabolism)
• DNA-Binding Proteins (chemistry, genetics, metabolism)
• Electrophoretic Mobility Shift Assay
• Mutation
• Mycobacterium tuberculosis (metabolism)
• Protein Binding
• Protein Structure, Quaternary