Langmuir, 24 (1), 69 -75, 2008. 10.1021/la702493u S0743-7463(70)02493-9
Web Release Date: November 30, 2007

Copyright © 2007 American Chemical Society

A Tetrafluorophenyl Activated Ester Self-Assembled Monolayer for the Immobilization of Amine-Modified Oligonucleotides

Matthew R. Lockett, Margaret F. Phillips, Jessica L. Jarecki, Dora Peelen, and Lloyd M. Smith*

Department of Chemistry, University of Wisconsin, 1101 University Avenue, Madison, Wisconsin 53706

Received August 13, 2007

In Final Form: September 28, 2007

Abstract:

A tetrafluorophenyl (TFP) ester-terminated self-assembled monolayer (SAM) for the fabrication of DNA arrays on gold surfaces is described. Activated ester SAMs are desirable for biomolecule array fabrication because they readily react with amine-containing molecules to form a stable amide linkage. N-Hydroxysuccinimide (NHS) ester SAMs are commonly used for this purpose but are subject to a competing hydrolysis side reaction, limiting their effectiveness under basic conditions. TFP was evaluated here as an alternative activated ester leaving group with a potentially greater stability under basic conditions. It is shown that TFP SAMs are much more stable to basic pH than their NHS analogs and are also more hydrophobic, which is an advantage in the fabrication of high-density spotted arrays. DNA arrays prepared on TFP SAMs at pH 10 have a 5-fold greater surface density of DNA molecules, reduced fluorescence background, and smaller spot radii than those prepared on NHS SAM analogs.


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