Straightforward Protein Immobilization on Sylgard 184 PDMS Microarray Surface

Kevin A. Heyries, Christophe A. Marquette,* and Loïc J. Blum
Laboratoire de Gnie Enzymatique et Biomolculaire, Institut de Chimie et Biochimie Molculaires et Supramolculaires, Universit Lyon 1 CNRS 5246 ICBMS, Btiment CPE, 43, Bd du 11 Novembre 1918, 69622 Villeurbanne, Cedex, France
Langmuir, 2007, 23 (8), pp 4523–4527
DOI: 10.1021/la070018o
Publication Date (Web): March 14, 2007
Copyright © 2007 American Chemical Society
*

 Corresponding author. E-mail:  christophe.marquette@univ-lyon1.fr.

Abstract

Abstract Image

In this work, a straightforward technique for protein immobilization on Sylgard 184 is described. The method consists of a direct transfer of dried protein/salt solutions to the PDMS interface during the polymer curing. Such non-conventional treatment of proteins was found to have no major negative consequence on their integrity. The mechanisms of this direct immobilization were investigated using a lysine modified dextran molecule as a model. Clear experimental results suggested that both chemical bounding and molding effect were implicated. As a proof of concept study, three different proteins were immobilized on a single microarray (Arachis hypogaea lectin, rabbit IgG, and human IgG) and used as antigens for capture of chemiluminescent immunoassays. The proteins were shown to be easily recognized by their specific antibodies, giving antibody detection limits in the fmol range.

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History

  • Published In Issue April 10, 2007
  • Received January 4, 2007

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