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红外激光烧蚀微采样在小体积蛋白质组学中的应用。

Infrared Laser Ablation Microsampling for Small Volume Proteomics.

机构信息

Department of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70803, United States.

出版信息

J Am Soc Mass Spectrom. 2022 Jun 1;33(6):1003-1010. doi: 10.1021/jasms.2c00063. Epub 2022 May 10.

Abstract

Infrared (IR) laser ablation was used to remove localized tissue regions from which proteins were extracted and processed with a low volume sample preparation workflow for bottom-up proteomics by liquid chromatography tandem mass spectrometry (LC-MS/MS). A polytetrafluoroethylene (PTFE) coated glass slide with 2 mm diameter microwells was used to capture ablated rat brain tissue for in situ protein digestion with submicroliter solution volumes. The resulting peptides were analyzed with LC-MS/MS for protein identification and label-free quantification. The method was used to identify an average of 600, 1350, and 1900 proteins from ablation areas of 0.01, 0.04, and 0.1 mm, respectively, from a 50 μm thick rat brain tissue section. Differential proteomics of 0.01 mm regions captured from cerebral cortex and corpus callosum was accomplished to demonstrate the capabilities of the approach.

摘要

红外(IR)激光烧蚀用于去除提取蛋白质的局部组织区域,并通过液相色谱串联质谱(LC-MS/MS)进行的体积小的样品制备工作流程进行自上而下的蛋白质组学处理。使用带有 2 毫米直径微孔的聚四氟乙烯(PTFE)涂层玻璃载玻片捕获烧蚀的大鼠脑组织,以进行亚微升溶液体积的原位蛋白质消化。用 LC-MS/MS 分析所得肽进行蛋白质鉴定和无标记定量。该方法平均可从 50μm 厚的大鼠脑组织切片中 0.01、0.04 和 0.1mm 的烧蚀区域鉴定出 600、1350 和 1900 种蛋白质。对从大脑皮层和胼胝体捕获的 0.01mm 区域进行差异蛋白质组学分析,以证明该方法的能力。

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