牛血清白蛋白
共价键
化学
石墨烯
酰胺
非共价相互作用
X射线光电子能谱
范德瓦尔斯力
疏水效应
氧化物
吸附
血清白蛋白
胺气处理
组合化学
高分子化学
烯丙胺
蛋白质吸附
共价结合
氧化胺
有机化学
氢键
作者
Shiva Shahriari,Santosh Panjikar,Rk Singh Raman,Murali Sastry
标识
DOI:10.1016/j.colsurfb.2025.115203
摘要
Developing robust, user-friendly platforms for protein and enzyme immobilisation is a key challenge in biomedical and industrial fields. Graphene oxide (GO) has emerged as a promising support for immobilising various biomolecules. This study explores both covalent and noncovalent immobilisation of bovine serum albumin (BSA) onto GO under varying conditions. Noncovalent immobilisation at different pH levels relies on electrostatic and hydrophobic interactions, hydrogen bonding, and van der Waals forces to form the GO-BSA complex. Covalent immobilisation involves activating GO's carboxyl groups with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide. hydrochloride (EDC) and stabilising with N-hydroxysuccinimide (NHS) to produce functionalised GO (FGO), which reacts with BSA's amine groups to form FGO-BSA conjugates. X-ray photoelectron spectroscopy (XPS) confirmed covalent binding through the detection of amide bonds and aromatic nitrogen. Interestingly, XPS also revealed higher BSA loading in GO-BSA (noncovalent) compared to FGO-BSA (covalent) under acidic conditions. Bradford assays further showed that GO can adsorb up to 80 % of introduced BSA via both immobilisation methods.
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