Université Paris-UMR CNRS - CSPBAT - LBPS - UFR SMBH, Bobigny, France.
J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Dec 1;879(31):3681-7. doi: 10.1016/j.jchromb.2011.10.006. Epub 2011 Oct 11.
It is known that protein adsorption is the initial interaction between implanted biomaterials and biological environment. Generally, a complex protein layer will be formed on material surfaces within a few minutes and the composition of this layer at the interface determines the biological response to the implanted material, and therefore the long-term compatibility of the biomaterial. Despite different techniques exist to observe protein adsorption on biomaterials, none of them led to the identification of adsorbed proteins. In this paper, we report a chromatographic technique coupled to proteomics to analyse and identify proteins from complex biological samples adsorbed on biomaterial surfaces. This approach is based on (1) elaboration of the chromatographic support containing the biomaterial (2) a chromatography step involving adsorption of proteins on the biomaterial (3) the high-resolution separation of eluted proteins by 2-DE gel and (4) the identification of proteins by mass spectrometry. Experiments were performed with proteins from platelets rich plasma (PRP) adsorbed on a biomaterial which consist in titanium bioactivated with PolyNaSS. Our results show that chromatographic approach combined to 2-DE gels and mass spectrometry provides a powerful tool for the analysis and identification of proteins adsorbed on various surfaces.
众所周知,蛋白质吸附是植入生物材料与生物环境的初始相互作用。通常,在几分钟内,材料表面会形成复杂的蛋白质层,该层在界面处的组成决定了对植入材料的生物学反应,进而决定了生物材料的长期相容性。尽管存在观察生物材料上蛋白质吸附的不同技术,但没有一种技术能够鉴定吸附的蛋白质。在本文中,我们报告了一种将色谱技术与蛋白质组学相结合的技术,用于分析和鉴定吸附在生物材料表面的复杂生物样品中的蛋白质。该方法基于:(1)包含生物材料的色谱支撑物的制备;(2)涉及蛋白质在生物材料上吸附的色谱步骤;(3)通过 2-DE 凝胶进行洗脱蛋白质的高分辨率分离;(4)通过质谱法鉴定蛋白质。实验是用富含血小板的血浆(PRP)中的蛋白质在经聚 NaSS 生物活化的钛生物材料上吸附进行的。我们的结果表明,将色谱方法与 2-DE 凝胶和质谱法相结合,为分析和鉴定各种表面上吸附的蛋白质提供了有力的工具。