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Proteomic Analysis of Biomaterial Surfaces after Contacting with Body Fluids by MALDI-ToF Mass Spectroscopy

机译:MALDI-TOF质谱与体液接触后的生物材料表面蛋白质组学分析

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We developed a method to identify proteins adsorbed on solid surfaces from a solution containing a complex mixture of proteins by using Matrix-Assisted Laser Desorption/Ionization-Time of Flight mass (MALDI-ToF mass) spectroscopy. In the method, we performed all procedures of peptide mass fingerprint method including denaturation, reduction, alkylation, digestion, and spotting of matrix on substrates. The method enabled us to avoid artifacts of pipetting that could induce changes in the composition. We also developed an algorithm to identify the adsorbed proteins. In this work, we demonstrate the identification of proteins adsorbed on self-assembled monolayers (SAMs). Our results show that the composition of proteins on the SAMs critically depends on the terminal groups of the molecules constituting the SAMs, indicating that the competitive adsorption of protein molecules is largely affected by protein-surface interaction. The method introduced here can provide vital information to clarify the mechanism underlying the responses of cells and tissues to biomaterials.
机译:我们开发了一种鉴定鉴定吸附在固体表面上的蛋白质通过使用基质辅助激光解吸/电离 - 飞行质量(MALDI-TOF质量)光谱分子的溶液含有含有蛋白质复杂混合物的溶液。在该方法中,我们进行了肽质量指纹方法的所有程序,包括在基材上的变性,还原,烷基化,消化和基质的斑点。该方法使我们能够避免引发的移液器的伪像,其可以诱导组合物的变化。我们还开发了一种识别吸附蛋白质的算法。在这项工作中,我们证明了吸附在自组装单层(SAMS)上吸附的蛋白质的鉴定。我们的研究结果表明,SAM上的蛋白质组成尺寸依赖性取决于构成SAMS的分子的末端基团,表明蛋白质分子的竞争吸附在很大程度上受蛋白质表面相互作用的影响。介绍的方法可以提供重要信息,以澄清细胞和组织对生物材料的反应的基础。

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