Synthetic Ligands for Modulating Bacterial Communication

该项目的主要目标是设计、合成和评价新的化学诱导剂， 调节细菌中的细胞间通讯机制。细菌与细菌之间交流的能力 他们自己和作为一个群体的作用在传染病的发展中至关重要。兰阴性 细菌使用小分子（或自诱导物）及其同源蛋白受体的化学“语言 来感知当地的人口密度，这种现象被称为“群体感应”。在人口众多的情况下 密度，病原菌使用这种传感机制组织成结构化的社区，称为 生物膜和激活毒力途径，是无数慢性感染的基础。发展 控制细菌群体感应和减弱生物膜形成的方法将产生重大影响 对人类健康的影响。我们假设合成配体可用于拦截细菌自身诱导物/ 受体结合并调节群体感应和生物膜形成。这一战略将使我们能够 解决细菌通讯领域的基本问题。首先，我们发现的配体 揭示了小分子促进或抑制的分子水平特征， 群体感应第二，合成配体可用于探测构象要求， 自身诱导物受体激活和失活。第三，定制的更高亲和力的配体将使分离成为可能。 众多的自我诱导物受体。我们已经开发了一种方法来解决这些问题 集成合成有机，组合和生物物理化学技术的问题，以快速 鉴定调节细菌群体感应的新分子。该研究计划有三个 具体目的：（1）设计和合成针对细菌自身诱导物受体的新配体，（2） 测试合成配体对相关病原菌群体感应的影响;（3） 使用现代生物技术表征非天然配体与自身诱导物受体的结合相互作用 生物物理技术我们已经验证了这种方法在我们的初步研究，通过合成 和鉴定一组新的群体感应小分子拮抗剂。 相关性：细菌使用化学信号引发大多数人类感染。的发现 阻断这些信号通路的方法将对公众健康产生深远的影响。有一个 全球迫切需要新的抗微生物疗法;通过 拦截细菌通信网络代表了一种全新的治疗方法， 临床及时

The broad goal of this project is the design, synthesis, and evaluation of new chemical inducers that modulate cell-cell communication mechanisms in bacteria. The ability of bacteria to communicate with themselves and function as a group is crucial in the development of infectious disease. Gram-negative bacteria use a chemical 'language' of small molecules (or autoinducers) and their cognate protein receptors to sense their local population densities in a phenomenon known as 'quorum sensing'. At high population densities, pathogenic bacteria use this sensing mechanism to organize into structured communities called biofilms and activate virulence pathways that are the basis for myriad chronic infections. The development of methods to control bacterial quorum sensing and attenuate biofilm formation would have a major impact on human health. We hypothesize that synthetic ligands can be used to intercept bacterial autoinducer/ receptor binding and modulate quorum sensing and biofilm formation. This strategy would allow us to address fundamental questions in the field of bacterial communication. First, the ligands we uncover will reveal the molecular level features that are essential for small molecule promotion or suppression of quorum sensing. Second, synthetic ligands could be used to probe the conformational requirements for autoinducer receptor activation and inactivation. Third, tailored higher affinity ligands would enable isolation of the numerous recalcitrant autoinducer receptors. We have developed an approach to address these questions that integrates synthetic organic, combinatorial, and biophysical chemistry techniques to rapidly identify new molecules that modulate quorum sensing in bacteria. The proposed research has three Specific Aims: (1) To design and synthesize new ligands that target bacterial autoinducer receptors, (2) To test the effects of the synthetic ligands on quorum sensing in relevant pathogenic bacteria, and (3) To characterize the binding interactions of non-native ligands with autoinducer receptors using modern biophysical techniques. We have validated this approach in our preliminary studies through the synthesis and identification of a set of new small molecule antagonists of quorum sensing. Relevance: Bacteria use chemical signals to initiate the majority of human infections. The discovery of methods to block these signaling pathways would have a profound impact on public health. There is an urgent, global need for new antimicrobial therapies; the ability to interfere with bacterial virulence by intercepting bacterial communication networks represents a completely new therapeutic approach and is clinically timely.