Applied and Plasma Physics, School of Physics (A28), University of Sydney, Sydney, NSW 2006, Australia.
Langmuir. 2011 May 17;27(10):6138-48. doi: 10.1021/la200376f. Epub 2011 Apr 14.
Horseradish peroxidase (HRP) was immobilized onto both plasticized and unplasticized polyvinylchloride (PVC) and ultrahigh molecular weight polyethylene (UHMWPE). Plasma immersion ion implantation (PIII) in a nitrogen plasma with 20 kV bias was used to facilitate covalent immobilization and to improve the wettability of the surfaces. The surfaces and immobilized protein were studied using attenuated total reflection infrared (ATR-IR) spectroscopy and water contact angle measurements. Protein elution on exposure to repeated sodium dodecyl sulfate (SDS) washing was used to assess the strength of HRP immobilization. The presence of low molecular weight components (plasticizer, additives in solvent, unreacted monomers, adsorbed molecules on surface) was found to have a major influence on the strength of immobilization and the conformation of the protein on the samples not exposed to the PIII treatment. A phenomenological model considering interactions between the low molecular weight components, the protein molecule, and the surface is developed to explain these observations.
辣根过氧化物酶(HRP)固定在增塑和未增塑的聚氯乙烯(PVC)和超高相对分子质量聚乙烯(UHMWPE)上。采用 20 kV 偏压的氮气等离子体体浸没离子注入(PIII)促进共价固定化并提高表面润湿性。使用衰减全反射红外(ATR-IR)光谱和水接触角测量来研究表面和固定化蛋白质。通过暴露于重复的十二烷基硫酸钠(SDS)洗涤来评估 HRP 固定化的强度。发现低分子量成分(增塑剂、溶剂中的添加剂、未反应的单体、表面吸附的分子)的存在对固定化强度和未经过 PIII 处理的样品上蛋白质的构象有重大影响。提出了一个考虑低分子量成分、蛋白质分子和表面之间相互作用的唯象模型来解释这些观察结果。