Young Aidan G, McQuillan A James, Green David P
Department of Chemistry, University of Otago, Dunedin, New Zealand.
Langmuir. 2009 Jul 7;25(13):7416-23. doi: 10.1021/la900350s.
Avidin-biotin bioconjugation reactions have been carried out on CdS nanoparticle films in H2O and D2O and investigated using in situ ATR-IR spectroscopic techniques. The experimental procedure involved the sequential adsorption of mercaptoacetic acid, the protein avidin, and the subsequent binding of the ligand biotin. The IR spectra of the solution-phase species mercaptoacetic acid, avidin, and biotin, at pH=7.2 were generally found to be similar in both H2O and D2O, with some minor peak shifts due to solvation changes. The IR spectra of the adsorbed species suggested that avidin may have undergone a conformational change upon adsorption to the CdS surface. In general, adsorption-induced conformational changes for avidin are likely, but to our knowledge have not been previously reported. The conformation of adsorbed avidin appeared to change again upon the binding of biotin, with the spectral data suggesting partial reversion to its native solution conformation.
已在水和重水中的硫化镉纳米颗粒薄膜上进行了抗生物素蛋白-生物素生物共轭反应,并使用原位衰减全反射红外光谱技术进行了研究。实验过程包括巯基乙酸、蛋白质抗生物素蛋白的顺序吸附,以及随后配体生物素的结合。通常发现,在pH = 7.2时,巯基乙酸、抗生物素蛋白和生物素的溶液相物种的红外光谱在水和重水中相似,由于溶剂化变化存在一些微小的峰位移。吸附物种的红外光谱表明,抗生物素蛋白在吸附到硫化镉表面时可能发生了构象变化。一般来说,抗生物素蛋白吸附诱导的构象变化是可能的,但据我们所知,此前尚未有报道。吸附的抗生物素蛋白的构象在生物素结合后似乎再次发生变化,光谱数据表明部分恢复到其天然溶液构象。