Department of Cell and Molecular Pharmacology & Experimental Therapeutics, Medical University of South Carolina, Charleston, SC, USA.
Methods Mol Biol. 2021;2271:331-342. doi: 10.1007/978-1-0716-1241-5_23.
N-glycan imaging mass spectrometry (N-glycan IMS) enables the detection and characterization of N-glycans in thin histological tissue sections. N-glycan IMS is used to study N-glycan regulation and localization in tissue-specific regions, such as tumor and normal adjacent to tumor, or by cell type within a tissue. Once a specific tissue-localized N-glycan signature is found to be associated with by a disease state, it has been challenging to study modulation of the same N-glycan signature by conventional molecular biology techniques. Here we describe a protocol that adapts tissue N-glycan IMS analysis workflows to cells grown on glass slides in an array format. Cells are grown under normal conditions in a cell culture chamber, fixed to maintain normal morphology, and sprayed with a thin coating of PNGase F to release N-glycans for imaging mass spectrometry profiling.
N-糖链成像质谱(N-glycan IMS)可用于检测和鉴定组织切片中的 N-糖链。N-glycan IMS 可用于研究组织中特定区域(如肿瘤和肿瘤附近的正常组织)或特定细胞类型中的 N-糖链的调控和定位。一旦发现与疾病状态相关的特定组织定位 N-糖链特征,使用传统分子生物学技术研究相同 N-糖链特征的调节就具有挑战性。在此,我们描述了一种方案,该方案将组织 N-糖链 IMS 分析工作流程适用于以阵列形式生长在载玻片上的细胞。细胞在细胞培养室内正常条件下生长,固定以保持正常形态,并用薄的 PNGase F 涂层喷涂,以释放用于成像质谱分析的 N-糖链。