A comparative analysis of polyurethane hydrogel for immobilization of IgG on chips

被引:26
作者
Derwinska, Katarzyna
Gheber, Levi A.
Preininger, Claudia [1 ]
机构
[1] Osterreich Forschungszentrum Seibersdorf GmbH, ARC, Dept Bioresources, A-2444 Seibersdorf, Austria
[2] Ben Gurion Univ Negev, Dept Biotechnol Engn, IL-84105 Beer Sheva, Israel
关键词
protein microarray; polyurethane; print buffer; antibody immobilization; ANTIBODY MICROARRAYS; SIGNAL ENHANCEMENT; PROTEIN; MICROCHIPS; ARRAYS;
D O I
10.1016/j.aca.2007.04.019
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Hydrogels are considered an optimum material for protein chip surfaces, since they provide a quasi-liquid environment which allows protein activity to be maintained and shows good spot morphology as well as excellent immobilization capacity. In the following, we present a polyurethane (PU) chip that electrostatically binds IgG. The PU surface is optimized with regard to layer thickness (similar to 200 nm), hydrogel (2%) and immobilized antibody concentration (0.5 mg mL(-1); 0.3 ng spot(-1)), pH and ionic strength of the print buffer as well as to blocking solution. Evaluation is done in a direct IgG immunoassay using the Nexterion slide H as a reference. It is shown that higher IgG loading is achieved on the PU chip than on slide H, no matter whether I x PBS (pH 7.2), Sorensen (pH 5.8) or Nexterion buffer was used as a spotting solution. Moreover, the crossreactivity with goat IgG, human IgG and monoclonal anti-CRP spotted in Nexterion buffer was as low as <= 0.74% (slide H: <= 3.34%). (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:132 / 138
页数:7
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