Xilin Gu, Peter J. Rowheder, Zanlin Yu, Alexander Mohapatra, Shichun Lun, Xiuju Jiang, Daqiang Li, Nicholas L. Yan, Tyler C. Detomasi, Daniel F. Torres Pomares, Yifei Chen, Jason E. Gestwicki, Gang Lin, William R. Bishai, Joel D. Ernst, Yifan Cheng, Charles S. Craik, Jason K. Sello
{"title":"Substrate Mimicry by Inhibitors of the Mycobacterium tuberculosis 20S Proteasome and Their Activity against Mycobacteria In Vitro and in Macrophages","authors":"Xilin Gu, Peter J. Rowheder, Zanlin Yu, Alexander Mohapatra, Shichun Lun, Xiuju Jiang, Daqiang Li, Nicholas L. Yan, Tyler C. Detomasi, Daniel F. Torres Pomares, Yifei Chen, Jason E. Gestwicki, Gang Lin, William R. Bishai, Joel D. Ernst, Yifan Cheng, Charles S. Craik, Jason K. Sello","doi":"10.1021/acschembio.6c00448","DOIUrl":null,"url":null,"abstract":"<p>The remarkable and problematic capacity of <em><em>Mycobacterium tuberculosis</em></em> to persist in the host is dependent on a functional 20S proteasome that is structurally and functionally analogous to its mammalian counterpart. It has been proposed that this enzyme is critical for the bacterium’s adaptive response to a variety of stressors in the host. Here, we report the structure of a rationally designed and species-selective inhibitor of the <em>Mtb</em> 20S proteasome in complex with the enzyme. The inhibitor was inspired by the syringolin natural products—covalent proteasome inhibitors that mimic a substrate. Structure elucidation of the <em>Mtb</em> 20S proteasome-inhibitor adduct via cryo-electron microscopy revealed that the inhibitor mimics a substrate yet engages the active site in a different fashion than the syringolin natural products. Corroboration of this model via the synthesis of hypothetical inhibitors led to the discovery of a more potent inhibitor, as evidenced in kinetic assays for enzyme inhibition. Both inhibitors are permeable to and active in <em><em>M. tuberculosis</em></em>. They sensitize the bacterium to chemically and pharmacologically induced nitrosative stress <em>in vitro</em>. Importantly, they suppress the persistence of live mycobacteria in murine and human macrophages.</p>","PeriodicalId":11,"journal":{"name":"ACS Chemical Biology","volume":"21 9","pages":"2275–2285"},"PeriodicalIF":3.6000,"publicationDate":"2026-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Chemical Biology","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acschembio.6c00448","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/12 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The remarkable and problematic capacity of Mycobacterium tuberculosis to persist in the host is dependent on a functional 20S proteasome that is structurally and functionally analogous to its mammalian counterpart. It has been proposed that this enzyme is critical for the bacterium’s adaptive response to a variety of stressors in the host. Here, we report the structure of a rationally designed and species-selective inhibitor of the Mtb 20S proteasome in complex with the enzyme. The inhibitor was inspired by the syringolin natural products—covalent proteasome inhibitors that mimic a substrate. Structure elucidation of the Mtb 20S proteasome-inhibitor adduct via cryo-electron microscopy revealed that the inhibitor mimics a substrate yet engages the active site in a different fashion than the syringolin natural products. Corroboration of this model via the synthesis of hypothetical inhibitors led to the discovery of a more potent inhibitor, as evidenced in kinetic assays for enzyme inhibition. Both inhibitors are permeable to and active in M. tuberculosis. They sensitize the bacterium to chemically and pharmacologically induced nitrosative stress in vitro. Importantly, they suppress the persistence of live mycobacteria in murine and human macrophages.
期刊介绍:
ACS Chemical Biology provides an international forum for the rapid communication of research that broadly embraces the interface between chemistry and biology.
The journal also serves as a forum to facilitate the communication between biologists and chemists that will translate into new research opportunities and discoveries. Results will be published in which molecular reasoning has been used to probe questions through in vitro investigations, cell biological methods, or organismic studies.
We welcome mechanistic studies on proteins, nucleic acids, sugars, lipids, and nonbiological polymers. The journal serves a large scientific community, exploring cellular function from both chemical and biological perspectives. It is understood that submitted work is based upon original results and has not been published previously.