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Spectroscopic and microscopic examination of protein adsorption and blocking of non-specific binding to silicon surfaces modified with APTES and GOPS

机译:光谱和显微镜检查蛋白质吸附和非特异性结合到经APTES和GOPS修饰的硅表面的非特异性结合

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摘要

X-ray Photoelectron Spectroscopy (XPS), Atomic Force Microscopy (AFM) and Time of Flight Secondary Ion Mass Spectrometry (TOF-SIMS) were applied to characterize two series of silicon nitride surfaces, modified either with (3-aminopropyl)triethoxysilane (APTES) or (3-glycidoxypropyl)trimethoxysilane (GOPS), prior to and after immobilization of rabbit gamma globulins (rIgG) at different concentrations and blocking with bovine serum albumin (BSA). Higher rIgG amount was adsorbed to surfaces silanized with APTES rather than GOPS, resulting in different behavior to subsequent blocking. There was no increase in total protein surface density due to blocking with BSA for surfaces with already high protein coverage. Apparently, BSA molecules were partly exchanged with rIgG ones, in case of APTES and higher rIgG concentrations, or attached to free surface sites, for GOPS modified surfaces.
机译:应用X射线光电子能谱(XPS),原子力显微镜(AFM)和飞行时间二次离子质谱(TOF-SIMS)来表征两个系列的氮化硅表面,这些表面经(3-氨基丙基)三乙氧基硅烷(APTES)改性)或(3-环氧丙氧基丙基)三甲氧基硅烷(GOPS),在固定不同浓度的兔γ球蛋白(rIgG)之前和之后用牛血清白蛋白(BSA)封闭。较高的rIgG量被吸附到用APTES而不是GOPS硅烷化的表面上,从而导致与随后的封闭行为不同。对于已经具有高蛋白覆盖率的表面,由于被BSA封闭,总蛋白表面密度没有增加。显然,在APTES和更高的rIgG浓度的情况下,对于GOPS修饰的表面,BSA分子被部分与rIgG交换,或附着在自由表面上。

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