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Identification of ligand analogues that control c-di-GMP riboswitches

机译:鉴定控制c-di-GMP核糖开关的配体类似物

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Riboswitches for the bacterial second messenger c-di-GMP control the expression of genes involved in numerous cellular processes such as virulence, competence, biofilm formation, and flagella synthesis. Therefore, the two known c-di-GMP riboswitch classes represent promising targets for developing novel modulators of bacterial physiology. Here, we examine the binding characteristics of circular and linear c-di-GMP analogues for representatives of both class I and II c-di-GMP riboswitches derived from the pathogenic bacterium Vibrio choleae (class I) and Clostridium difficile (class II). Some compounds exhibit values for apparent dissociation constant (K _D) below 1 μM and associate with riboswitch RNAs during transcription with a speed that is sufficient to influence riboswitch function. These findings are consistent with the published structural models for these riboswitches and suggest that large modifications at various positions on the ligand can be made to create novel compounds that target c-di-GMP riboswitches. Moreover, we demonstrate the potential of an engineered allosteric ribozyme for the rapid screening of chemical libraries for compounds that bind c-di-GMP riboswitches.
机译:细菌第二信使c-di-GMP的核糖开关控制参与许多细胞过程(如毒力,能力,生物膜形成和鞭毛合成)的基因的表达。因此,两个已知的c-di-GMP核糖开关类别代表了开发新型细菌生理调节剂的有希望的目标。在这里,我们检查了圆形和线性c-di-GMP类似物的结合特性,它们分别代表源自致病性细菌霍乱弧菌(I类)和艰难梭菌(II类)的I类和II类c-di-GMP核糖开关。一些化合物表现出低于1μM的表观解离常数(K_D)值,并在转录过程中与核糖开关RNA缔合,其速度足以影响核糖开关功能。这些发现与已公开的这些核糖开关的结构模型是一致的,并且表明可以对配体上的各个位置进行大的修饰以产生靶向c-di-GMP核糖开关的新型化合物。此外,我们证明了工程化的变构核酶对化学文库中与c-di-GMP核糖开关结合的化合物的快速筛选的潜力。

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