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Inhibiting the VIM-2 Metallo-beta-Lactamase by Graphene Oxide and Carbon Nanotubes

机译:氧化石墨烯和碳纳米管抑制VIM-2金属β-内酰胺酶

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摘要

Metallo-beta-lactamases (MBLs) degrade a broad spectrum of antibiotics including the latest carbapenems. So far, limited success has been achieved in developing its inhibitors using small organic molecules. VIM-2 is one of the most studied and important MBLs. In this work, we screened 10 nanomaterials, covering a diverse range of surface properties including charge, hydrophobicity, and specific chemical bonding. Among these, graphene oxide and carbon nanotubes are the most potent inhibitors, while most other materials do not show much inhibition effect. The inhibition is noncompetitive and is attributed to the hydrophobic interaction with the enzyme. Adsorption of VIM-2 was further probed using protein displacement assays where it cannot displace or be displaced by bovine serum albumin (BSA). This information is useful for rational design inhibitors for MBLs and more specific inhibition might be achieved by further surface modifications on these nanocarbons.
机译:金属β-内酰胺酶(MBL)可降解包括最新碳青霉烯类在内的多种抗生素。迄今为止,在使用小有机分子开发其抑制剂方面取得的成功有限。 VIM-2是研究最多且最重要的MBL之一。在这项工作中,我们筛选了10种纳米材料,涵盖了各种表面性质,包括电荷,疏水性和特定的化学键合。其中,氧化石墨烯和碳纳米管是最有效的抑制剂,而大多数其他材料则没有太大的抑制作用。该抑制是非竞争性的,并且归因于与酶的疏水相互作用。使用蛋白质置换测定法进一步检测VIM-2的吸附,在该置换法中,VIM-2不能置换或不能被牛血清白蛋白(BSA)置换。此信息对于MBL的合理设计抑制剂很有用,并且可以通过对这些纳米碳进行进一步的表面修饰来实现更具体的抑制作用。

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