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一种具有疗效的新型肌动蛋白结合药物。

A Novel Actin Binding Drug with Efficacy.

机构信息

Department of Biology, Texas A&M University, College Station, Texas, USA.

Department of Chemistry and Biochemistry, CPRIT Synthesis and Drug-Lead Discovery Laboratory, Baylor University, Waco, Texas, USA.

出版信息

Antimicrob Agents Chemother. 2018 Dec 21;63(1). doi: 10.1128/AAC.01585-18. Print 2019 Jan.

Abstract

Occidiofungin is produced by the soil bacterium MS14 and is structurally similar or identical to the burkholdines, xylocandins, and cepacidines. This study identified the primary cellular target of occidiofungin, which was determined to be actin. The modification of occidiofungin with a functional alkyne group enabled affinity purification assays and localization studies in yeast. Occidiofungin has a subtle effect on actin dynamics that triggers apoptotic cell death. We demonstrate the highly specific localization of occidiofungin to cellular regions rich in actin in yeast and the binding of occidiofungin to purified actin Furthermore, a disruption of actin-mediated cellular processes, such as endocytosis, nuclear segregation, and hyphal formation, was observed. All of these processes require the formation of stable actin cables, which are disrupted following the addition of a subinhibitory concentration of occidiofungin. We were also able to demonstrate the effectiveness of occidiofungin in treating a vulvovaginal yeast infection in a murine model. The results of this study are important for the development of an efficacious novel class of actin binding drugs that may fill the existing gap in treatment options for fungal infections or different types of cancer.

摘要

氧环杀真菌素由土壤细菌 MS14 产生,其结构与伯克霍尔德菌素、木霉素和头孢菌素相似或相同。本研究确定了氧环杀真菌素的主要细胞靶标,即肌动蛋白。用功能化炔基对氧环杀真菌素进行修饰,使亲和纯化测定和酵母中的定位研究成为可能。氧环杀真菌素对肌动蛋白动力学有细微影响,可引发细胞凋亡。我们证明了氧环杀真菌素在酵母中高度特异地定位于富含肌动蛋白的细胞区域,并证明了氧环杀真菌素与纯化的肌动蛋白结合。此外,观察到细胞内过程如内吞作用、核分离和菌丝形成的中断。所有这些过程都需要形成稳定的肌动蛋白纤维,而在添加亚抑制浓度的氧环杀真菌素后,这些纤维会被破坏。我们还能够在小鼠模型中证明氧环杀真菌素治疗阴道酵母菌感染的有效性。本研究的结果对于开发一种有效的新型肌动蛋白结合药物具有重要意义,这种药物可能填补真菌或不同类型癌症治疗方案的现有空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9317/6325233/4990dcd9f8b4/AAC.01585-18-f0001.jpg

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