Orechovich Institute of Biomedical Chemistry of RAMS, Moscow, Russia.
Proteomics. 2012 Nov;12(22):3295-8. doi: 10.1002/pmic.201200135. Epub 2012 Nov 2.
We describe an experimental approach for direct molecular fishing of prey protein on the surface of two types of paramagnetic particles (PMP) having different size and composition. Human microsomal cytochrome b(5) (b(5)) and its known partner human cytochrome P450 3A5 (CYP3A5) were used as bait and prey proteins, respectively. For assessing the level of unspecific binding of background proteins, α-fetoprotein (aFP) was used. SPR measurements were applied for quantitative analysis of trapped proteins (CYP3A5 and aFP) after fishing on PMP. It was shown that the described approach of molecular fishing on micro-PMP provides enough prey proteins for LC-MS/MS identification and SPR validation, so this approach can be used for discovery of new protein-protein interactions in the framework of Human Proteome Project.
我们描述了一种实验方法,用于直接在两种具有不同大小和组成的顺磁颗粒 (PMP) 的表面上捕获猎物蛋白质。用人微粒体细胞色素 b(5) (b(5)) 和已知的其伴侣人类细胞色素 P450 3A5 (CYP3A5) 分别作为诱饵和猎物蛋白质。为了评估背景蛋白质非特异性结合的水平,使用了α-胎蛋白 (aFP)。在 PMP 上进行分子捕捞后,通过 SPR 测量对捕获的蛋白质 (CYP3A5 和 aFP) 进行定量分析。结果表明,微 PMP 上分子捕捞的描述方法为 LC-MS/MS 鉴定和 SPR 验证提供了足够的猎物蛋白质,因此该方法可用于在人类蛋白质组计划框架内发现新的蛋白质-蛋白质相互作用。