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荧光素-5-硫代半卡巴腙作为一种探针,可直接在活细胞内对粘蛋白型 O-连接糖蛋白进行成像。

Fluorescein-5-thiosemicarbazide as a probe for directly imaging of mucin-type O-linked glycoprotein within living cells.

机构信息

Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, College of Life Science, Northwest University, Xi'an, People's Republic of China.

出版信息

Glycoconj J. 2012 Aug;29(5-6):445-52. doi: 10.1007/s10719-012-9425-y. Epub 2012 Jul 15.

Abstract

Mucin-type O-linked glycoproteins are known for regulating many aspects of cell activity but remains a challenge to detect under physiological conditions which is due to the diversity of O-glycosylation and the lack of universal method. Here a direct labeling strategy for in situ visualizing of mucin-type O-linked glycoproteins on living cells has been developed. The strategy utilizes the combination of metabolic engineering and chemical probing technologies. Treating cells with an unnatural sugar, 2-keto Ac(4)GalNAc analogue (2-keto isostere of GalNAc) to generate keto groups upon cells, followed by chemoselective ligation of keto groups on cells with a fluorescent tag, fluorescein-5-thiosemicarbazide (FTSC), provides a promising platform to probing mucin-type O-glycosylation on living cells. The FTSC conjugates illustrated very similar fluorescent spectra as FITC, a fluorescent tag widely used in proteomics, indicating good compatibility with commonly used fluorescent equipments. The established method eliminated the need of an additional fluorescent amplification step. Cells after being treated with the method maintained a rather high level of viability of 84.3%. Finally, the assay has been successfully applied to image the expression of mucin-type O-linked glycoproteins within CHO and HeLa cells.

摘要

黏蛋白型 O-链接糖蛋白以调控细胞活动的多个方面而闻名,但由于 O-糖基化的多样性和缺乏通用方法,在生理条件下检测它们仍然具有挑战性。在此,开发了一种用于在活细胞上原位可视化黏蛋白型 O-链接糖蛋白的直接标记策略。该策略利用代谢工程和化学探测技术的结合。用非天然糖 2-酮基 Ac(4)GalNAc 类似物(GalNAc 的酮类似物)处理细胞,在细胞内生成酮基,然后用荧光标记物荧光素-5-硫代半卡巴腙(FTSC)对细胞上的酮基进行化学选择性连接,为在活细胞上探测黏蛋白型 O-糖基化提供了一个很有前景的平台。FTSC 缀合物的荧光光谱与 FITC 非常相似,FITC 是蛋白质组学中广泛使用的荧光标记物,这表明与常用的荧光设备具有良好的兼容性。所建立的方法消除了对额外荧光放大步骤的需求。用该方法处理后的细胞保持相当高的活力,为 84.3%。最后,该测定法已成功应用于 CHO 和 HeLa 细胞内黏蛋白型 O-链接糖蛋白的表达成像。

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