Kilarski Witold W, Herbert John, Bikfalvi Andreas
Institute for Molecular Engineering, The University of Chicago, Chicago, IL, USA.
Institute of Integrative Biology, University of Liverpool, Liverpool, UK.
Methods Mol Biol. 2018;1722:31-56. doi: 10.1007/978-1-4939-7553-2_3.
We present a protocol for the specific labeling and isolation of proteins from the membrane surface of endothelial cells and the surrounding extracellular matrix of organs, experimental wounds and tumors using chicken embryos. Proteins are deglycosylated on streptavidin resin and purified after gentle elution and trypsin digestion. Peptides are analyzed by spectroscopy and reverse proteomic fingerprinting. The major advantages of this protocol include reductions in both the background and overrepresentation of single proteins that would otherwise mask less well-represented proteins in the mass spectroscopy analysis. We also present methods to identify putative vascular and endothelial cell targets from isolated chicken membranes and extracellular proteins. The use of human genome and transcriptome data facilitates this analysis. Human orthologs of isolated chicken proteins are identified using best hit BLAST searches against the Human Reference Sequence Database. The expression of Human orthologs is then assessed for endothelial and non-endothelial cell enrichment using second generation RNA-seq sequenced libraries. Scanning of the published literature then provides a ranking score of those genes most likely involved in cancer or having a link to angiogenesis.
我们展示了一种使用鸡胚从内皮细胞膜表面以及器官、实验性伤口和肿瘤周围的细胞外基质中特异性标记和分离蛋白质的方案。蛋白质在链霉亲和素树脂上进行去糖基化处理,经温和洗脱和胰蛋白酶消化后进行纯化。肽段通过光谱分析和反向蛋白质组指纹识别进行分析。该方案的主要优点包括减少背景干扰以及单一蛋白质的过度富集,否则这些单一蛋白质会在质谱分析中掩盖含量较低的蛋白质。我们还展示了从分离的鸡膜和细胞外蛋白质中鉴定假定的血管和内皮细胞靶点的方法。人类基因组和转录组数据的使用有助于此分析。使用针对人类参考序列数据库的最佳匹配BLAST搜索来鉴定分离的鸡蛋白质的人类直系同源物。然后使用第二代RNA测序文库评估人类直系同源物在内皮细胞和非内皮细胞中的富集表达。对已发表文献的检索随后提供了那些最有可能参与癌症或与血管生成相关的基因的排名分数。