TY - JOUR
T1 - Two efficient polymeric chemical platforms for oligonucleotide microarray preparation
AU - Consolandi, Clarissa
AU - Castiglioni, Bianca
AU - Bordoni, Roberta
AU - Busti, Elena
AU - Battaglia, Cristina
AU - Bernardi, Luigi Rossi
AU - De Bellis, Gianluca
PY - 2002
Y1 - 2002
N2 - In this report we describe two robust procedures for oligonucleotide microarray preparation based on polymeric coatings. The proposed chemical approaches include: 1) a glass functionalisation step with appropriate silanes (γ-aminopropyltriethoxysilane-APTES or 3-glycid-oxypropyltrimethoxysilane-GOPS), 2) a coating step using polymers (poly-L-Lysine or poly(acrylic acid-co-acrylamide) copolymer) covalently bound to the modified glass and 3) a surface activation step to allow for the attachment of amino-modified oligonucleotides. Results obtained using these chemistries in oligo microarray preparation show: 1) an overall high loading capacity and availability to hybridisation against targets, 2) a good uniformity, 3) resistance to consecutive probing/stripping cycles, 4) stability to thermal cycles, 5) effectiveness in hybridisation-mediated mutation detection procedures and 6) the possibility to perform enzymatic reactions, such as ligation.
AB - In this report we describe two robust procedures for oligonucleotide microarray preparation based on polymeric coatings. The proposed chemical approaches include: 1) a glass functionalisation step with appropriate silanes (γ-aminopropyltriethoxysilane-APTES or 3-glycid-oxypropyltrimethoxysilane-GOPS), 2) a coating step using polymers (poly-L-Lysine or poly(acrylic acid-co-acrylamide) copolymer) covalently bound to the modified glass and 3) a surface activation step to allow for the attachment of amino-modified oligonucleotides. Results obtained using these chemistries in oligo microarray preparation show: 1) an overall high loading capacity and availability to hybridisation against targets, 2) a good uniformity, 3) resistance to consecutive probing/stripping cycles, 4) stability to thermal cycles, 5) effectiveness in hybridisation-mediated mutation detection procedures and 6) the possibility to perform enzymatic reactions, such as ligation.
KW - Amino-modified oligonucleotides
KW - Mutation detection
KW - Oligo-microarrays
UR - http://www.scopus.com/inward/record.url?scp=1842845771&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=1842845771&partnerID=8YFLogxK
U2 - 10.1081/NCN-120015069
DO - 10.1081/NCN-120015069
M3 - Article
C2 - 12484451
AN - SCOPUS:1842845771
SN - 0732-8311
VL - 21
SP - 561
EP - 580
JO - Nucleosides and Nucleotides
JF - Nucleosides and Nucleotides
IS - 8-9
ER -