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PMID: 11302753 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Nearly instantaneous, cation-independent, high selectivity nucleic acid hybridization to DNA microarrays.

Biochemical and biophysical research communications ·Vol. 282 ·No. 5 ·2001-04-20 ·Pages 1263-7

Belosludtsev Y, Belosludtsev I, Iverson B, Lemeshko S, Wiese R, Hogan M, Powdrill T

Abstract

Hybridization rate enhancement has been demonstrated for high molecular weight DNA target binding to a microarray. Microarrays were fabricated using biotin-modified oligonucleotides complexed with streptavidin (SA), which serves as an attachment to the underlying surface. It is shown that at low salt and pH 5, where SA develops a positive charge, duplex formation becomes at least 80-fold faster than seen under standard conditions, where SA is neutral or anionic. Duplex formation becomes independent of solution state cation concentration in the low pH state, under conditions where specificity remains high. The utility of such applied surface science is discussed.

MeSH Terms
Biotin/chemistry Cations/chemistry Fluorescent Dyes Hydrogen-Ion Concentration Molecular Chaperones/chemistry Nucleic Acid Conformation Nucleic Acid Hybridization/methods Oligonucleotide Array Sequence Analysis/economics,instrumentation,methods Oligonucleotides/chemistry Osmolar Concentration Polystyrenes/chemistry Sensitivity and Specificity Streptavidin/chemistry Surface Properties Time Factors
Chemicals
Cations Fluorescent Dyes Molecular Chaperones Oligonucleotides Polystyrenes Biotin Streptavidin
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Belosludtsev Y
Genometrix Inc., The Woodlands, Texas 77381, USA. [email protected]
Belosludtsev I
Iverson B
Lemeshko S
Wiese R
Hogan M
Powdrill T
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
2001-04-20
Pages
1263-7
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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