Suppr超能文献

一种使用福尔马林固定石蜡包埋切片从单病例获取综合蛋白质组学数据的方案。

A Protocol for the Acquisition of Comprehensive Proteomics Data from Single Cases Using Formalin-Fixed Paraffin Embedded Sections.

作者信息

Acland Mitchell, Mittal Parul, Arentz Georgia, Whitehead Fergus, Hoffmann Peter, Klingler-Hoffmann Manuela, Oehler Martin K

机构信息

Adelaide Proteomics Centre, School of Biological Sciences, The University of Adelaide, Adelaide, SA 5005, Australia.

Clinical & Health Science, Mawson Lakes Campus, University of South Australia, Adelaide, SA 5095, Australia.

出版信息

Methods Protoc. 2022 Jul 10;5(4):57. doi: 10.3390/mps5040057.

Abstract

The molecular analysis of small or rare patient tissue samples is challenging and often limited by available technologies and resources, such as reliable antibodies against a protein of interest. Although targeted approaches provide some insight, here, we describe the workflow of two complementary mass spectrometry approaches, which provide a more comprehensive and non-biased analysis of the molecular features of the tissue of interest. Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) generates spatial intensity maps of molecular features, which can be easily correlated with histology. Additionally, liquid chromatography tandem mass spectrometry (LC-MS/MS) can identify and quantify proteins of interest from a consecutive section of the same tissue. Here, we present data from concurrent precancerous lesions from the endometrium and fallopian tube of a single patient. Using this complementary approach, we monitored the abundance of hundreds of proteins within the precancerous and neighboring healthy regions. The method described here represents a useful tool to maximize the number of molecular data acquired from small sample sizes or even from a single case. Our initial data are indicative of a migratory phenotype in these lesions and warrant further research into their malignant capabilities.

摘要

对少量或罕见的患者组织样本进行分子分析具有挑战性,并且常常受到现有技术和资源的限制,例如缺乏针对感兴趣蛋白质的可靠抗体。尽管靶向方法能提供一些见解,但在此我们描述了两种互补质谱方法的工作流程,这两种方法能对感兴趣组织的分子特征进行更全面且无偏差的分析。基质辅助激光解吸/电离(MALDI)质谱成像(MSI)可生成分子特征的空间强度图,这些图能轻松与组织学相关联。此外,液相色谱串联质谱(LC-MS/MS)可从同一组织的连续切片中鉴定和定量感兴趣的蛋白质。在此,我们展示了来自一名患者子宫内膜和输卵管同时存在的癌前病变的数据。使用这种互补方法,我们监测了癌前区域和相邻健康区域内数百种蛋白质的丰度。这里描述的方法是一种有用的工具,可最大限度地从少量样本甚至单个病例中获取分子数据。我们的初步数据表明这些病变具有迁移表型,值得对其恶性能力进行进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c24/9326557/0bce1ea0c1db/mps-05-00057-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验