TY - JOUR
T1 - Differential receptors create patterns diagnostic for ATP and GTP
AU - McCleskey, Shawn C.
AU - Griffin, Michael J.
AU - Schneider, Stephen E.
AU - McDevitt, John T.
AU - Anslyn, Eric V.
PY - 2003/2/5
Y1 - 2003/2/5
N2 - Herein we report the combination of a library of resin-bound sensors along with a multicomponent sensor array. This novel combinatorial array sensor system shows selectivity for nucleotide phosphates in solution. The design of the anchored receptor includes a 1,3,5-trisubstituted-2,4,6-triethylbenzene scaffold coupled with peptide libraries. Each chemosensor is placed into a micromachined cavity within a silicon wafer, and the optical changes observed by a charged-coupled device result in near-real-time digital analysis of solutions. A colorimetric displacement assay was performed, and time-dependent imaging studies of the selected sensing ensembles result in a differential responses upon addition of adenosine 5′-triphosphate (ATP), adenosine 5′-monophosphate (AMP), or guanosine 5′-triphosphate (GTP). An advantage to this approach is that it creates an array of sensors that gives a fingerprint response for each analyte. Principal component analysis indicates that the library of chemosensors can differentiate between ATP, GTP, and AMP. On the basis of factor loading values, individual sensors from the library were sequenced to elucidate their chemical composition.
AB - Herein we report the combination of a library of resin-bound sensors along with a multicomponent sensor array. This novel combinatorial array sensor system shows selectivity for nucleotide phosphates in solution. The design of the anchored receptor includes a 1,3,5-trisubstituted-2,4,6-triethylbenzene scaffold coupled with peptide libraries. Each chemosensor is placed into a micromachined cavity within a silicon wafer, and the optical changes observed by a charged-coupled device result in near-real-time digital analysis of solutions. A colorimetric displacement assay was performed, and time-dependent imaging studies of the selected sensing ensembles result in a differential responses upon addition of adenosine 5′-triphosphate (ATP), adenosine 5′-monophosphate (AMP), or guanosine 5′-triphosphate (GTP). An advantage to this approach is that it creates an array of sensors that gives a fingerprint response for each analyte. Principal component analysis indicates that the library of chemosensors can differentiate between ATP, GTP, and AMP. On the basis of factor loading values, individual sensors from the library were sequenced to elucidate their chemical composition.
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U2 - 10.1021/ja021230b
DO - 10.1021/ja021230b
M3 - Article
C2 - 12553782
AN - SCOPUS:0037419786
SN - 0002-7863
VL - 125
SP - 1114
EP - 1115
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 5
ER -