TY - JOUR
T1 - A novel fluorescent biosensor for Adenosine Triphosphate detection based on the polydopamine nanospheres integrating with enzymatic recycling amplification
AU - Ji, Xiaoting
AU - Yi, Bingqing
AU - Xu, Yujuan
AU - Zhao, Yanan
AU - Zhong, Hua
AU - Ding, Caifeng
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017/7/1
Y1 - 2017/7/1
N2 - Based on the protective performance of polydopamine nanospheres (PDANSs) for DNA against nuclease digestion and the specific recognition characteristic of aptamer, we have developed an enzymatic recycling signal amplification method for highly sensitive and selective detection of adenosine triphosphate (ATP). Fluorescence measurements were carried out to verify the DNA polymerase and exonuclease III (Exo III) assisted target recycling process and fluorescence signal amplification. In the absence of the ATP, initially, the signal DNA-PDANSs complex was in the “off” state due to the efficient fluorescence quenching of 6-carboxyfluorescein (FAM) adjacent to the surface of PDANSs. Due to the binding of the aptamer by ATP, it trigger DNA polymerase and Exo III assisted target recycling process by the product of release, the complex would change into the “on” state as a result of the dissociation of the FAM from the surface of PDANSs, thus providing greatly enhanced fluorescence emission intensity. The method allows quantitative detection of ATP in the range of 20–600 nM with a detection limit of 8.32 nM. This biosensor requires no complex operations, and is a new high efficiency method for ATP detection.
AB - Based on the protective performance of polydopamine nanospheres (PDANSs) for DNA against nuclease digestion and the specific recognition characteristic of aptamer, we have developed an enzymatic recycling signal amplification method for highly sensitive and selective detection of adenosine triphosphate (ATP). Fluorescence measurements were carried out to verify the DNA polymerase and exonuclease III (Exo III) assisted target recycling process and fluorescence signal amplification. In the absence of the ATP, initially, the signal DNA-PDANSs complex was in the “off” state due to the efficient fluorescence quenching of 6-carboxyfluorescein (FAM) adjacent to the surface of PDANSs. Due to the binding of the aptamer by ATP, it trigger DNA polymerase and Exo III assisted target recycling process by the product of release, the complex would change into the “on” state as a result of the dissociation of the FAM from the surface of PDANSs, thus providing greatly enhanced fluorescence emission intensity. The method allows quantitative detection of ATP in the range of 20–600 nM with a detection limit of 8.32 nM. This biosensor requires no complex operations, and is a new high efficiency method for ATP detection.
KW - Exonuclease III (Exo III)
KW - Fluorescence resonance energy transfer (FRET)
KW - Polydopamine nanospheres (PDANSs)
KW - Polymerase, recycling amplification
UR - http://www.scopus.com/inward/record.url?scp=85015752866&partnerID=8YFLogxK
U2 - 10.1016/j.talanta.2017.03.052
DO - 10.1016/j.talanta.2017.03.052
M3 - Article
C2 - 28411826
AN - SCOPUS:85015752866
SN - 0039-9140
VL - 169
SP - 8
EP - 12
JO - Talanta
JF - Talanta
ER -