Department of Chemistry, Materials and Chemical Engineering Giulio Natta, Politecnico di Milano, Via Mancinelli 7, 20131 Milano, Italy.
J Proteomics. 2011 Nov 18;74(12):2856-65. doi: 10.1016/j.jprot.2011.06.033. Epub 2011 Jul 20.
The use of Cibacron Blue columns (HiTrapBlue) in proteome analysis for removal of plasma albumin, for facilitating biomarker discovery, has not borne any fruit. In fact, the visibility of low-abundance proteins was obscured. It is here reported that, upon albumin sequestering from plasma, there is adsorption, via hydrophobic interaction, of a substantial number of plasma proteins, which are lost for subsequent analysis if the blue resin is eluted via an ion shock (2 M NaCl) or with a somewhat more robust eluant (5 M urea, 2 M thiourea, 2% CHAPS, 2% sulphobetain 3-10) as recommended by manufacturers. Such treatments, in fact, release at most 25 to 30 unique gene products, including albumin. If, however, the Affigel-Blue resin, after elution with either of the two above eluants, is further eluted with boiling 4% SDS in 25 mM DTT, all the missing proteins (amounting to at least 112 unique species) are desorbed and biomarker analysis can be conducted in a correct way. It is also suggested that such blue-resin treatment could be coupled to ProteoMiner adsorption, this coupled treatment further enhancing the chances of success for discovery of low-abundance proteins.
在蛋白质组学分析中,使用 Cibacron Blue 柱(HiTrapBlue)去除血浆白蛋白,以促进生物标志物的发现,但并未取得任何成果。事实上,低丰度蛋白质的可见度受到了影响。本文报道了在从血浆中分离白蛋白后,通过疏水相互作用吸附了大量的血浆蛋白,如果使用离子冲击(2 M NaCl)或制造商推荐的更具强度的洗脱液(5 M 尿素、2 M 硫脲、2% CHAPS、2% sulphobetain 3-10)从蓝色树脂洗脱,这些蛋白会丢失,无法进行后续分析。事实上,这些处理方法最多只能释放 25 到 30 种独特的基因产物,包括白蛋白。然而,如果在使用上述两种洗脱液之一洗脱 Affigel-Blue 树脂后,再用 25 mM DTT 中的 4% SDS 煮沸进一步洗脱,则所有缺失的蛋白质(至少有 112 种独特物种)都会被解吸,并且可以正确地进行生物标志物分析。本文还建议将这种蓝色树脂处理与 ProteoMiner 吸附结合,这种联合处理可以进一步提高发现低丰度蛋白质的成功率。