首页> 外文会议>Institution of Engineering and Technology Seminar on MEMS Sensors and Actuators >DIRECT ADSORPTION OF CHEMICALLY MODIFIED BIOMOLECULES ONTO GOLD: A RAPID METHOD FOR BIOLOGICAL FUNCTIONALIZATION OF MEMS
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DIRECT ADSORPTION OF CHEMICALLY MODIFIED BIOMOLECULES ONTO GOLD: A RAPID METHOD FOR BIOLOGICAL FUNCTIONALIZATION OF MEMS

机译:将化学改性的生物分子直接吸附到金中:一种快速的MEMS生物官能化方法

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The present work reports a simple, rapid and versatile strategy for glycoprotein immobilization, based on the targeted functionalization of carbohydrate residues with disulphide "anchors" derivatives able to spontaneously chemisorb onto gold, with no need of surface pre-functionalization. Different glycoproteins as enzymes and antibodies were chemically modified using this "one step" bio-immobilization protocol and directly adsorbed onto gold coated interfaces. Surface plasmon resonance (SPR) and Electrochemistry techniques revealed that direct adsorption of a modified glyco-enzyme (horseradish peroxidase) onto gold led to the formation of a densely packed SAM, where each single biomolecule is several thousand times more active than a non modified one. In the case of antibodies, the specific location of the carbohydrate moieties in the constant region resulted in the formation of active and site-oriented SAMs. This bio-immobilization method was applied to the bio-functionalization of a degenerate mode MEMS sensor (MEMSens). Preliminary results obtained for the detection of protein S-100ββ (brain injury marker), indicate a promising low detection limit.
机译:本报告展开的工作简单,快速和灵活的战略,糖蛋白固定化,基于与二硫化碳“锚”能够自发地化学吸附到衍生品黄金的糖残基的针对性功能化,无需表面预功能化。使用该“一步”生物固定方案和直接吸附在金涂覆的界面上,将不同的糖蛋白作为酶和抗体进行化学修饰。表面等离子体共振(SPR)和电化学技术表明,将改性的甘醇 - 酶(辣根过氧化物酶)直接吸附到金LED上,形成密集包装的山姆,其中每种生物分子比未改进的一个更活跃的数千倍。在抗体的情况下,恒定区域中碳水化合物部分的特定位置导致形成活性和位点导向的SAMS。将该生物固定化方法应用于退化模式MEMS传感器(Memsens)的生物官能化。用于检测蛋白质S-100ββ(脑损伤标志物)的初步结果表明有前景的低检测限。

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