Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC 27695, USA.
Biochemistry. 2012 Dec 11;51(49):9776-8. doi: 10.1021/bi3015289. Epub 2012 Nov 29.
2-Aminoimidazoles (2AIs) have been documented to disrupt bacterial protection mechanisms, including biofilm formation and genetically encoded antibiotic resistance traits. Using Acinetobacter baumannii, we provide initial insight into the mechanism of action of a 2AI-based antibiofilm agent. Confocal microscopy confirmed that the 2AI is cell permeable, while pull-down assays identified BfmR, a response regulator that is the master controller of biofilm formation, as a target for this compound. Binding assays demonstrated specificity of the 2AI for response regulators, while computational docking provided models for 2AI-BfmR interactions. The 2AI compound studied here represents a unique small molecule scaffold that targets bacterial response regulators.
2-氨基咪唑(2AIs)已被证明可以破坏细菌的保护机制,包括生物膜形成和遗传编码的抗生素耐药性特征。我们使用鲍曼不动杆菌,初步了解了基于 2AI 的抗生物膜剂的作用机制。共焦显微镜证实 2AI 可穿透细胞,而下拉实验则确定了 BfmR,一种生物膜形成的主控制器,是该化合物的靶标。结合实验证明了 2AI 对响应调节剂的特异性,而计算对接提供了 2AI-BfmR 相互作用的模型。本研究中研究的 2AI 化合物代表了一种独特的小分子支架,可靶向细菌响应调节剂。