Suppr超能文献

真菌 1,3-β-葡聚糖合酶的结构。

Structure of a fungal 1,3-β-glucan synthase.

机构信息

Department of Biochemistry and Biophysics, School of Basic Medical Sciences, Peking University, Beijing, China.

State Key Laboratory of Female Fertility Promotion, Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, China.

出版信息

Sci Adv. 2023 Sep 15;9(37):eadh7820. doi: 10.1126/sciadv.adh7820. Epub 2023 Sep 13.

Abstract

1,3-β-Glucan serves as the primary component of the fungal cell wall and is produced by 1,3-β-glucan synthase located in the plasma membrane. This synthase is a molecular target for antifungal drugs such as echinocandins and the triterpenoid ibrexafungerp. In this study, we present the cryo-electron microscopy structure of 1,3-β-glucan synthase (Fks1) at 2.47-Å resolution. The structure reveals a central catalytic region adopting a cellulose synthase fold with a cytosolic conserved GT-A-type glycosyltransferase domain and a closed transmembrane channel responsible for glucan transportation. Two extracellular disulfide bonds are found to be crucial for Fks1 enzymatic activity. Through structural comparative analysis with cellulose synthases and structure-guided mutagenesis studies, we gain previously unknown insights into the molecular mechanisms of fungal 1,3-β-glucan synthase.

摘要

1,3-β-葡聚糖是真菌细胞壁的主要成分,由位于质膜上的 1,3-β-葡聚糖合酶产生。这种合酶是棘白菌素类和三萜类伊博苷类等抗真菌药物的分子靶标。在这项研究中,我们呈现了 1,3-β-葡聚糖合酶(Fks1)在 2.47-Å 分辨率下的冷冻电镜结构。该结构揭示了一个采用纤维素合酶折叠的中央催化区域,具有胞质保守的 GT-A 型糖基转移酶结构域和一个封闭的跨膜通道,负责葡聚糖的运输。发现两个细胞外二硫键对于 Fks1 的酶活性至关重要。通过与纤维素合酶的结构比较分析和结构导向的突变研究,我们获得了对真菌 1,3-β-葡聚糖合酶的分子机制的先前未知的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f09c/10499315/50607a6e177c/sciadv.adh7820-f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验