| Literature DB >> 19170514 |
A Jasper Nijdam1, Michael R Zianni, Edward E Herderick, Mark M-C Cheng, Jenifer R Prosperi, Fredika A Robertson, Emanuel F Petricoin, Lance A Liotta, Mauro Ferrari.
Abstract
Physicochemically modified silicon substrates can provide a high quality alternative to nitrocellulose-coated glass slides for use in reverse-phase protein microarrays. Enhancement of protein microarray sensitivities is an important goal, especially because molecular targets within patient tissues exist in low abundance. The ideal array substrate has a high protein binding affinity and low intrinsic background signal. Silicon, which has low intrinsic autofluorescence, is being explored as a potential microarray surface. In a previous paper ( Nijdam , A. J. ; Cheng , M. M.-C. ; Fedele , R. ; Geho , D. H. ; Herrmann , P. ; Killian , K. ; Espina , V. ; Petricoin , E. F. ; Liotta , L. A. ; Ferrari , M. Physicochemically Modified Silicon as Substrate for Protein Microarrays . Biomaterials 2007 , 28 , 550 - 558 ), it is shown that physicochemical modification of silicon substrates increases the binding of protein to silicon to a level comparable with that of nitrocellulose. Here, we apply such substrates in a reverse-phase protein microarray setting in two model systems.Entities:
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Year: 2009 PMID: 19170514 PMCID: PMC2693459 DOI: 10.1021/pr800455y
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466