TY - JOUR
T1 - Highly sensitive fluorometric Hg2+ biosensor with a mercury(II)-specific oligonucleotide (MSO) probe and water-soluble graphene oxide (WSGO)
AU - Liu, Xingfen
AU - Miao, Likun
AU - Jiang, Xu
AU - Ma, Yanwen
AU - Fan, Quli
AU - Huang, Wei
PY - 2011/5
Y1 - 2011/5
N2 - A highly sensitive and selective, "turn-on" and simple Hg 2+ biosensor is reported by using water-soluble graphene oxide (WSGO) and dye-labeled mercury(II)-specific oligonucleotide (MSO) probe. The probe is rich of thymine (T) and can readily form the stem-loop structure which consists of the T-Hg2+-T configuration. In the absence of Hg2+, the probe exists as a random coil conformation which can be readily adsorbed on the surface of WSGO by strong noncovalent binding of bases, as a result, the fluorescence of the dye labeled on the terminus of the MSO is strongly quenched by the efficient electron/energy transfer from the dye to WSGO. Upon addition of Hg2+, the formation of the T-Hg2+-T structure releases the MSO from the surface of WSGO, resulting in a restoration of the fluorescence of dye-labeled MSO probe. Based on this observation, a highly sensitive and selective Hg2+ sensor is developed, which can work with "turn-on" mode in aqueous solutions at room temperature. By using the fluorometric method, the limit of detection for Hg2+ can reach picomolar range (187 pmol·L-1), and it is demonstrated that the biosensor is highly selective and only minimally perturbed by a wide range of non-specific metal ions.
AB - A highly sensitive and selective, "turn-on" and simple Hg 2+ biosensor is reported by using water-soluble graphene oxide (WSGO) and dye-labeled mercury(II)-specific oligonucleotide (MSO) probe. The probe is rich of thymine (T) and can readily form the stem-loop structure which consists of the T-Hg2+-T configuration. In the absence of Hg2+, the probe exists as a random coil conformation which can be readily adsorbed on the surface of WSGO by strong noncovalent binding of bases, as a result, the fluorescence of the dye labeled on the terminus of the MSO is strongly quenched by the efficient electron/energy transfer from the dye to WSGO. Upon addition of Hg2+, the formation of the T-Hg2+-T structure releases the MSO from the surface of WSGO, resulting in a restoration of the fluorescence of dye-labeled MSO probe. Based on this observation, a highly sensitive and selective Hg2+ sensor is developed, which can work with "turn-on" mode in aqueous solutions at room temperature. By using the fluorometric method, the limit of detection for Hg2+ can reach picomolar range (187 pmol·L-1), and it is demonstrated that the biosensor is highly selective and only minimally perturbed by a wide range of non-specific metal ions.
KW - Biosensor
KW - Fluorescence
KW - Graphene
KW - Mercury
UR - http://www.scopus.com/inward/record.url?scp=79957570875&partnerID=8YFLogxK
U2 - 10.1002/cjoc.201190175
DO - 10.1002/cjoc.201190175
M3 - 文章
AN - SCOPUS:79957570875
SN - 1001-604X
VL - 29
SP - 1031
EP - 1035
JO - Chinese Journal of Chemistry
JF - Chinese Journal of Chemistry
IS - 5
ER -