Miniaturized Digestion and Extraction of Surface Proteins from Candida albicans following Treatment with Histatin 5 for Mass Spectrometry Analysis

Shirley Fan, E. Moffa, Yizhi Xiao, W. Siqueira, K. Yeung
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Abstract

A common approach to isolate surface proteins from fungal and bacterial cells is to perform a proteolytic cleavage of proteins on the surface of intact cells suspended in solution. This paper describes miniaturization of this technique, in which cells are adhered on glass surfaces, and all sample treatments are conducted at μL volumes. Specifically, Candida albicans cells were attached onto HSA-coated glass slides. By depositing the appropriate reagent solutions on the adhered cells, we successfully performed cell washing, treatment with antifugal peptide, Histatin 5, and a proteolysis on intact cells with trypsin. The resulting peptides were subsequently analysed by mass spectrometry. In general, the data obtained was similar to that collected with suspended cells in much larger sample volumes. However, our miniaturized workflow offers the benefit of greatly reducing the consumption of cells and reagents.
组蛋白5处理后白色念珠菌表面蛋白的微型消化和提取用于质谱分析
从真菌和细菌细胞中分离表面蛋白质的一种常用方法是对悬浮在溶液中的完整细胞表面的蛋白质进行蛋白质水解裂解。本文描述了该技术的小型化,其中细胞粘附在玻璃表面,所有样品处理都在μL体积下进行。具体地说,将白色念珠菌细胞附着在hsa涂层的玻璃载玻片上。通过将合适的试剂溶液沉积在粘附的细胞上,我们成功地进行了细胞洗涤,抗真菌肽,组蛋白5处理,以及胰蛋白酶对完整细胞的蛋白水解。所得肽随后用质谱法分析。总的来说,获得的数据与在更大的样本量中用悬浮细胞收集的数据相似。然而,我们的小型化工作流程提供了大大减少细胞和试剂消耗的好处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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