（SCI）Screening Peptide Inhibitors Using Phage Peptide Library with Isocitrate Lyase in Mycobacterium tuberculosis as Target

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• Affiliation of Author(s):化学与生命科学学院
• Teaching and Research Group:化学与生命科学学院
• Journal:CHEMICAL RESEARCH IN CHINESE UNIVERSITES
• Funded by:自选课题
• Key Words:Mycobacterium tuberculosis Isocitrate lyase Gene expression Phage peptide library Peptide inhibitor
• Abstract:When devoured by macrophages, Mycobacterium tuberculosis remains persistent in macrophages and gains energy through the glyoxylate bypass to maintain its long-term existence in host cells. Therefore it is possible to stop persistent infections by interdicting the glyoxylate bypass in which the isocitrate lyase(ICL) is the key rate-limiting enzyme and a persistence factor. ICL is the target of anti-TB(TB: tubercular) drugs, which could screen ICL out and effectively inhibit the activity of ICL in Mycobacterium tuberculosis, and because of this, anti-TB drugs can be used to kill persistent Mycobacterium tuberculosis. In this study, the ICL gene of the Mycobacterium tuberculosis H37Rv was cloned successfully and recombinant protein with bioactivity was obtained through the enzyme characteristic appraisal. The specific activity of the recombined ICL is 24 μmol·mg–1 ·min–1. The recombined ICL protein was used as the target, and phages which can specifically combine to ICL were screened in the phage 7 peptide library. According to the results of the ELISA and DNA sequence detection, eventually three 7-peptide chains were synthesized. Then the peptide chains were reacted with ICL, respectively, to detect their inhibitory effects on ICL. The results show that all the three 7-peptide chains possessed varying inhibitory effects on the activity of ICL. This study provided lead compounds for the research and development of new peptide anti-TB drugs.
• First Author:carter
• Indexed by:Journal paper
• Volume:27
• Issue:4
• Page Number:1
• Number of Words:1
• ISSN No.:1005-9040
• Translation or Not:no
• CN No.:22-1183/O6
• Date of Publication:2011-06-29