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用α2,6-唾液酸类似物选择性外切酶标记淋病奈瑟菌的脂寡糖。

Selective Exoenzymatic Labeling of Lipooligosaccharides of Neisseria gonorrhoeae with α2,6-Sialoside Analogues.

机构信息

Department of Chemical Biology and Drug Discovery Utrecht Institute for Pharmaceutical Sciences and Bijvoet Center for Biomedical Research, Utrecht University, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands.

Department of Biomolecular Health Sciences, Utrecht University, Yalelaan 1, 3584 CL, Utrecht, The Netherlands.

出版信息

Chembiochem. 2022 Oct 6;23(19):e202200340. doi: 10.1002/cbic.202200340. Epub 2022 Aug 23.

Abstract

The interactions between bacteria and their host often rely on recognition processes that involve host or bacterial glycans. Glycoengineering techniques make it possible to modify and study the glycans on the host's eukaryotic cells, but only a few are available for the study of bacterial glycans. Here, we have adapted selective exoenzymatic labeling (SEEL), a chemical reporter strategy, to label the lipooligosaccharides of the bacterial pathogen Neisseria gonorrhoeae, using the recombinant glycosyltransferase ST6Gal1, and three synthetic CMP-sialic acid derivatives. We show that SEEL treatment does not affect cell viability and can introduce an α2,6-linked sialic acid with a reporter group on the lipooligosaccharides by Western blot, flow cytometry and fluorescent microscopy. This new bacterial glycoengineering technique allows for the precise modification, here with α2,6-sialoside derivatives, and direct detection of specific surface glycans on live bacteria, which will aid in further unravelling the precise biological functions of bacterial glycans.

摘要

细菌与其宿主之间的相互作用通常依赖于涉及宿主或细菌糖的识别过程。糖基工程技术使得对宿主真核细胞上的聚糖进行修饰和研究成为可能,但可用于研究细菌聚糖的技术却寥寥无几。在这里,我们通过使用重组糖基转移酶 ST6Gal1 和三种合成的 CMP-唾液酸衍生物,对细菌病原体淋病奈瑟氏球菌的脂寡糖进行了选择性外切酶标记(SEEL),这是一种化学报告策略。我们表明,SEEL 处理不会影响细胞活力,并且可以通过 Western blot、流式细胞术和荧光显微镜在脂寡糖上引入带有报告基团的α2,6 连接的唾液酸。这种新的细菌糖基工程技术可实现精确修饰(此处为α2,6-唾液酸衍生物),并直接检测活细菌上特定的表面聚糖,这将有助于进一步揭示细菌聚糖的精确生物学功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c01/9804176/283f8c33c27b/CBIC-23-0-g004.jpg

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