Corgier Benjamin P, Bellon Sophie, Anger-Leroy Marielle, Blum Loïc J, Marquette Christophe A
Laboratoire de Génie Enzymatique et Biomoléculaire, Institut de Chimie et Biochimie Moléculaires et Supramoléculaires Université Lyon 1, CNRS 5246 ICBMS Batiment CPE, 43, bd du 11 novembre 1918, 69622 Villeurbanne, Cedex, France.
Langmuir. 2009 Aug 18;25(16):9619-23. doi: 10.1021/la900762s.
A direct protein immobilization method for surface plasmon resonance imaging (SPRi) gold chip arraying is exposed. The biomolecule electroaddressing strategy, previously demonstrated by our team on carbon surfaces, is here valuably involved and adapted to create a straightforward and efficient protein immobilization process onto SPRi-biochips. The proteins, modified with an aryl-diazonium adduct, are addressed to the SPRi chip surface through the electroreduction of the aryl-diazonium. The biomolecule deposition was followed through SPRi live measurements during the electrografting process. A specially designed setup enabled us to directly observe the mass increasing at the sensor surface while the proteins were electrografted. A pin electrospotting method, allowing the achievement of distinct sensing layers on gold SPRi-biochips, was used to generate microarray biochips. The integrity of the immobilized proteins and the specificity of the detection, based on antigen/antibody interactions, were demonstrated for the detection of specific antibodies and ovalbumin. The SPRi detection limit of ovalbumin using the electroaddressing of anti-ovalbumin IgG was compared with two other immobilization procedures, cystamine-glutaraldehyde self-assembled monolayer and pyrrole, and was found to be a decade lower than these ones (100 ng/mL, i.e., 2 nM).
公开了一种用于表面等离子体共振成像(SPRi)金芯片阵列的直接蛋白质固定方法。我们团队之前在碳表面证明的生物分子电寻址策略,在此被有效地采用并进行了调整,以在SPRi生物芯片上创建一种直接且高效的蛋白质固定过程。用芳基重氮加合物修饰的蛋白质通过芳基重氮的电还原作用被寻址到SPRi芯片表面。在电接枝过程中,通过SPRi实时测量跟踪生物分子的沉积。一种专门设计的装置使我们能够在蛋白质进行电接枝时直接观察传感器表面质量的增加。一种允许在金SPRi生物芯片上实现不同传感层的针式电点样方法被用于生成微阵列生物芯片。基于抗原/抗体相互作用,证明了固定化蛋白质的完整性和检测的特异性,用于检测特异性抗体和卵清蛋白。将使用抗卵清蛋白IgG电寻址的卵清蛋白的SPRi检测限与另外两种固定方法(胱胺 - 戊二醛自组装单层和吡咯)进行了比较,发现比它们低一个数量级(100 ng/mL,即2 nM)。