Elucidation of critical chemical moieties of metallo-β-lactamase inhibitors and prioritisation of target metallo-β-lactamases

被引:0
|
作者
Lee, Jung Hun [1 ]
Kim, Sang-Gyu [2 ]
Jang, Kyung-Min [1 ]
Shin, Kyoungmin [1 ]
Jin, Hyeonku [1 ]
Kim, Dae-Wi [2 ]
Jeong, Byeong Chul [1 ]
Lee, Sang Hee [1 ]
机构
[1] Myongji Univ, Dept Biol Sci, Natl Leading Res Lab Drug Resistance Prote, Yongin 17058, South Korea
[2] Jeonbuk Natl Univ, Div Life Sci, Jeonju, South Korea
基金
新加坡国家研究基金会;
关键词
Metallo-beta-lactamase inhibitor; chemical moiety; metallo-beta-lactamase variant type; BROAD-SPECTRUM INHIBITORS; IN-VITRO; STRUCTURAL INSIGHTS; CAPTOPRIL ANALOGS; ACID-DERIVATIVES; CALCIUM-EDTA; MURINE MODEL; ZINC-BINDING; NDM-1; ASPERGILLOMARASMINE;
D O I
10.1080/14756366.2024.2318830
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The urgent demand for effective countermeasures against metallo-beta-lactamases (MBLs) necessitates development of novel metallo-beta-lactamase inhibitors (MBLIs). This study is dedicated to identifying critical chemical moieties within previously developed MBLIs, and critical MBLs should serve as the target in MBLI evaluations. Using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), a systematic literature analysis was conducted, and the NCBI RefSeq genome database was exploited to access the abundance profile and taxonomic distribution of MBLs and their variant types. Through the implementation of two distinct systematic approaches, we elucidated critical chemical moieties of MBLIs, providing pivotal information for rational drug design. We also prioritised MBLs and their variant types, highlighting the imperative need for comprehensive testing to ensure the potency and efficacy of the newly developed MBLIs. This approach contributes valuable information to advance the field of antimicrobial drug discovery. [GRAPHICS]
引用
收藏
页数:13
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