Cranfield Health, Cranfield University, Cranfield, Bedfordshire, UK.
Biosens Bioelectron. 2010 Jan 15;25(5):1049-55. doi: 10.1016/j.bios.2009.09.030. Epub 2009 Oct 12.
The immobilisation of bio-receptors on transducer surfaces is a key step in the development of biosensors. The immobilisation needs to be fast, cheap and most importantly should not affect the biorecognition activity of the immobilised receptor. The development of a protocol for biomolecule immobilisation onto a surface plasmon resonance (SPR) sensor surface using inexpensive polythiol compounds is presented here. The method used here is based on the reaction between primary amines and thioacetal groups, formed upon reaction of o-phthaldialdehyde (OPA) and thiol compounds. The self-assembled thiol monolayers were characterised using contact angle and XPS. The possibility to immobilise proteins on monolayers was assessed by employing BSA as a model protein. For the polythiol layers exhibiting the best performance, a general protocol was optimised suitable for the immobilisation of enzymes and antibodies such as anti-prostate specific antigen (anti-PSA) and anti Salmonella typhimurium. The kinetic data was obtained for PSA binding to anti-PSA and for S. typhimurium cells with a detection limit of 5x10(6) cells mL(-1) with minimal non-specific binding of other biomolecules. These findings make this technique a very promising alternative for amine coupling compared to peptide bond formation. Additionally, it offers opportunity for immobilising proteins (even those with low isoelectric point) on neutral polythiol layers without any activation step.
生物受体在传感器表面的固定化是生物传感器发展的关键步骤。固定化需要快速、廉价,最重要的是不应影响固定化受体的生物识别活性。本文介绍了一种使用廉价的多硫醇化合物将生物分子固定在表面等离子体共振(SPR)传感器表面上的方案。这里使用的方法基于伯胺与硫代缩醛基团之间的反应,该反应是由邻苯二醛(OPA)和硫醇化合物反应形成的。自组装的硫醇单层使用接触角和 XPS 进行了表征。通过使用 BSA 作为模型蛋白来评估蛋白质在单层上固定的可能性。对于表现出最佳性能的多硫醇层,优化了适用于酶和抗体(如抗前列腺特异性抗原(抗 PSA)和抗鼠伤寒沙门氏菌)固定化的通用方案。获得了 PSA 与抗 PSA 结合以及 S. typhimurium 细胞结合的动力学数据,检测限为 5x10(6)个细胞 mL(-1),其他生物分子的非特异性结合最小。这些发现使得与肽键形成相比,该技术成为胺偶联的一种很有前途的替代方法。此外,它为在中性多硫醇层上固定化蛋白质(甚至那些等电点较低的蛋白质)提供了机会,而无需任何激活步骤。