Grube Christopher D, Roy Hervé
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, USA.
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, USA
J Biomol Screen. 2016 Aug;21(7):722-8. doi: 10.1177/1087057116642987. Epub 2016 Apr 12.
The transfer RNA (tRNA)-dependent pathway for lipid aminoacylation is a two-step pathway composed of (1) a tRNA aminoacylation step catalyzed by an aminoacyl-tRNA synthetase, forming a specific aa-tRNA, and (2) a tRNA-dependent transfer step in which the amino acid acylating the tRNA is transferred to an acceptor lipid. The latter step is catalyzed by a transferase located within the cytoplasmic membrane of certain bacteria. Lipid aminoacylation modifies the biochemical properties of the membrane and enhances resistance of some pathogens to various classes of antimicrobial agents and components of the innate immune response. Lipid aminoacylation has also been linked to increased virulence of various pathogenic bacteria. Inhibition of this mechanism would render pathogens more susceptible to existing drugs or to natural defenses of a host organism. Because lipid aminoacylation is widespread in many bacterial genera and absent from eukaryotes, and because the tRNA aminoacylation step of this pathway is also used in protein biosynthesis (a process essential for bacterial life), this pathway represents an attractive target for drug design. We have reconstituted the lipid aminoacylation pathway in vitro and optimized it for high-throughput screening of libraries of compounds to simultaneously identify inhibitors targeting each step of the pathway in a single assay.
脂质氨酰化的依赖转运RNA(tRNA)途径是一个两步途径,由以下步骤组成:(1)由氨酰-tRNA合成酶催化的tRNA氨酰化步骤,形成特定的氨酰-tRNA;(2)一个依赖tRNA的转移步骤,其中使tRNA氨酰化的氨基酸被转移到受体脂质上。后一步骤由位于某些细菌细胞质膜内的转移酶催化。脂质氨酰化改变了膜的生化特性,并增强了一些病原体对各类抗菌剂和先天免疫反应成分的抗性。脂质氨酰化还与多种病原菌的毒力增加有关。抑制这一机制会使病原体对现有药物或宿主生物体的天然防御更敏感。由于脂质氨酰化在许多细菌属中广泛存在而在真核生物中不存在,并且由于该途径的tRNA氨酰化步骤也用于蛋白质生物合成(细菌生命所必需的过程),因此该途径是药物设计的一个有吸引力的靶点。我们已经在体外重建了脂质氨酰化途径,并对其进行了优化,用于对化合物文库进行高通量筛选,以便在单一测定中同时鉴定针对该途径每个步骤的抑制剂。