| Literature DB >> 24440232 |
María González-González1, Raquel Bartolome1, Ricardo Jara-Acevedo2, Juan Casado-Vela3, Noelia Dasilva1, Sergio Matarraz1, Jacinto García4, J A Alcazar4, J M Sayagues1, Alberto Orfao5, Manuel Fuentes6.
Abstract
Antibody arrays hold great promise for biomedical applications, but they are typically manufactured using chemically functionalized surfaces that still require optimization. Here, we describe novel hetero-functionally activated glass surfaces favoring oriented antibody binding for improved performance in protein microarray applications. Antibody arrays manufactured in our facility using the functionalization chemistries described here proved to be reproducible and stable and also showed good signal intensities. As a proof-of-principle of the glass surface functionalization protocols described in this article, we built antibody-based arrays functionalized with different chemistries that enabled the simultaneous detection of 71 human leukocyte membrane differentiation antigens commonly found in peripheral blood mononuclear cells. Such detection is specific and semi-quantitative and can be performed in a single assay under native conditions. In summary, the protocol described here, based on the use of antibody array technology, enabled the concurrent detection of a set of membrane proteins under native conditions in a specific, selective, and semi-quantitative manner and in a single assay.Entities:
Keywords: Antibody arrays; Antibody immobilization; Functionalized surfaces; Protein microarrays; Surface functionalization
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Year: 2014 PMID: 24440232 DOI: 10.1016/j.ab.2014.01.002
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365