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A novel aptasensor for the ultra-sensitive detection of adenosine triphosphate via aptamer/quantum dot based resonance energy transferElectronic supplementary information (ESI) available. See DOI: 10.1039/c3an00449j

We designed a novel aptamer based biosensor (aptasensor) for ultrasensitive detection of adenosine triphosphate (ATP) through resonance energy transfer (RET). The ATP aptamer was modified with Cy3 at the 3′ end, and a green quantum dot (525) was attached to the 5′ end of its complementary sequence r...

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Main Authors: Li, Zheng, Wang, Yijing, Liu, Ying, Zeng, Yongyi, Huang, Aimin, Peng, Niancai, Liu, Xiaolong, Liu, Jingfeng
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creator Li, Zheng
Wang, Yijing
Liu, Ying
Zeng, Yongyi
Huang, Aimin
Peng, Niancai
Liu, Xiaolong
Liu, Jingfeng
description We designed a novel aptamer based biosensor (aptasensor) for ultrasensitive detection of adenosine triphosphate (ATP) through resonance energy transfer (RET). The ATP aptamer was modified with Cy3 at the 3′ end, and a green quantum dot (525) was attached to the 5′ end of its complementary sequence respectively. The ATP aptamer and its complementary sequence could assemble into a duplex structure in the absence of target ATP, and then decrease the distance between the quantum dot and Cy3 which could produce significant RET signal. Upon ATP binding, the ATP aptamer could dissociate with its complementary sequence and then increase the distance between the quantum dot and Cy3 which would significantly decrease the RET signal. Therefore, the ATP detection could be easily achieved through detection of the fluorescence intensity ratio between 525 nm and 560 nm. The results show that the emission fluorescence intensity ratio of 525/560 is linearly related to the logarithmic concentration of ATP. The linear range of this aptasensor is from 0.1 nM to 1 μM, and the detection limit is lower down to 0.01 nM. Excellent selectivity of this aptasensor for ATP has been demonstrated through the detection of thymidine triphosphate (TTP), cytidine triphosphate (CTP), guanosine triphosphate (GTP) and adenosine diphosphate (ADP) respectively as control. The method we described here could easily detect ATP with excellent selectivity, linearity and sensitivity down to the nanomolar range, as well as avoid photobleaching. Ultrasensitive quantitative detection of ATP through an aptasensor based on quantum dot resonance energy transfer.
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See DOI: 10.1039/c3an00449j</title><source>Royal Society of Chemistry</source><creator>Li, Zheng ; Wang, Yijing ; Liu, Ying ; Zeng, Yongyi ; Huang, Aimin ; Peng, Niancai ; Liu, Xiaolong ; Liu, Jingfeng</creator><creatorcontrib>Li, Zheng ; Wang, Yijing ; Liu, Ying ; Zeng, Yongyi ; Huang, Aimin ; Peng, Niancai ; Liu, Xiaolong ; Liu, Jingfeng</creatorcontrib><description>We designed a novel aptamer based biosensor (aptasensor) for ultrasensitive detection of adenosine triphosphate (ATP) through resonance energy transfer (RET). The ATP aptamer was modified with Cy3 at the 3′ end, and a green quantum dot (525) was attached to the 5′ end of its complementary sequence respectively. The ATP aptamer and its complementary sequence could assemble into a duplex structure in the absence of target ATP, and then decrease the distance between the quantum dot and Cy3 which could produce significant RET signal. Upon ATP binding, the ATP aptamer could dissociate with its complementary sequence and then increase the distance between the quantum dot and Cy3 which would significantly decrease the RET signal. Therefore, the ATP detection could be easily achieved through detection of the fluorescence intensity ratio between 525 nm and 560 nm. The results show that the emission fluorescence intensity ratio of 525/560 is linearly related to the logarithmic concentration of ATP. The linear range of this aptasensor is from 0.1 nM to 1 μM, and the detection limit is lower down to 0.01 nM. Excellent selectivity of this aptasensor for ATP has been demonstrated through the detection of thymidine triphosphate (TTP), cytidine triphosphate (CTP), guanosine triphosphate (GTP) and adenosine diphosphate (ADP) respectively as control. The method we described here could easily detect ATP with excellent selectivity, linearity and sensitivity down to the nanomolar range, as well as avoid photobleaching. 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Therefore, the ATP detection could be easily achieved through detection of the fluorescence intensity ratio between 525 nm and 560 nm. The results show that the emission fluorescence intensity ratio of 525/560 is linearly related to the logarithmic concentration of ATP. The linear range of this aptasensor is from 0.1 nM to 1 μM, and the detection limit is lower down to 0.01 nM. Excellent selectivity of this aptasensor for ATP has been demonstrated through the detection of thymidine triphosphate (TTP), cytidine triphosphate (CTP), guanosine triphosphate (GTP) and adenosine diphosphate (ADP) respectively as control. The method we described here could easily detect ATP with excellent selectivity, linearity and sensitivity down to the nanomolar range, as well as avoid photobleaching. Ultrasensitive quantitative detection of ATP through an aptasensor based on quantum dot resonance energy transfer.</abstract><doi>10.1039/c3an00449j</doi><tpages>5</tpages></addata></record>
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title A novel aptasensor for the ultra-sensitive detection of adenosine triphosphate via aptamer/quantum dot based resonance energy transferElectronic supplementary information (ESI) available. See DOI: 10.1039/c3an00449j
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