Crystal structure of AmpC BER and molecular docking lead to the discovery of broad inhibition activities of halisulfates against β-lactamases
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Title
- Crystal structure of AmpC BER and molecular docking lead to the discovery of broad inhibition activities of halisulfates against β-lactamases
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Author(s)
- Jeong, Bo-Gyeong; Na, Jung-Hyun; Bae, Da-Woon; Park, Soo-Bong; Lee, Hyi Seung; Cha, Sun-Shin
- KIOST Author(s)
- Lee, Hyi Seung(이희승)
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Alternative Author(s)
- 이희승
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Publication Year
- 2021-01
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Abstract
- AmpC BER is an extended-spectrum (ES) class C β-lactamase with a two-amino-acid insertion in the H10 helix region located at the boundary of the active site compared with its narrow spectrum progenitor. The crystal structure of the wild-type AmpC BER revealed that the insertion widens the active site by restructuring the flexible H10 helix region, which is the structural basis for its ES activity. Besides, two sulfates originated from the crystallization solution were observed in the active site. The presence of sulfate-binding subsites, together with the recognition of ring-structured chemical scaffolds by AmpC BER, led us to perform in silico molecular docking experiments with halisulfates, natural products isolated from marine sponge. Inspired by the snug fit of halisulfates within the active site, we demonstrated that halisulfate 3 and 5 significantly inhibit ES class C β-lactamases. Especially, halisulfate 5 is comparable to avibactam in terms of inhibition efficiency; it inhibits the nitrocefin-hydrolyzing activity of AmpC BER with a Ki value of 5.87 μM in a competitive manner. Furthermore, halisulfate 5 displayed moderate and weak inhibition activities against class A and class B/D enzymes, respectively. The treatment of β-lactamase inhibitors (BLIs) in combination with β-lactam antibiotics is a working strategy to cope with infections by pathogens producing ES β-lactamases. Considering the emergence and dissemination of enzymes insensitive to clinically-used BLIs, the broad inhibition spectrum and structural difference of halisulfates would be used to develop novel BLIs that can escape the bacterial resistance mechanism mediated by β-lactamases. © 2020
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ISSN
- 2001-0370
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URI
- https://sciwatch.kiost.ac.kr/handle/2020.kiost/41371
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DOI
- 10.1016/j.csbj.2020.12.015
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Bibliographic Citation
- COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, v.19, pp.145 - 152, 2021
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Publisher
- Elsevier B.V.
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Subject
- TRANSITION-STATE ANALOG; EXTENDED SUBSTRATE SPECTRUM; AMINO-ACID INSERTION; SESTERTERPENE SULFATES; HYDROLYSIS
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Keywords
- Crystal structure; AmpC BER; R2 loop; Marine natural products; Halisulfates; Broad-spectrum competitive inhibitors
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Type
- Article
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Language
- English
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Document Type
- Article
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