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Weak Binding of Levamisole by the Cocaine-Binding Aptamer Does Not Interfere with an Aptamer-Based Detection Assay
被引:4
|作者:
Shoara, Aron A.
[1
,2
]
Churcher, Zachary R.
[1
,2
]
Slavkovic, Sladjana
[1
,2
]
Johnson, Philip E.
[1
,2
]
机构:
[1] York Univ, Dept Chem, Toronto, ON M3J 1P3, Canada
[2] York Univ, Ctr Res Biomol Interact, Toronto, ON M3J 1P3, Canada
来源:
基金:
加拿大自然科学与工程研究理事会;
关键词:
LIGAND-BINDING;
STEM LENGTH;
NMR;
D O I:
10.1021/acsomega.1c03781
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Levamisole is a common and harmful adulterant of street samples of cocaine and can cause electrochemical tests for cocaine to give false negative results. To see if levamisole would interfere with aptamer-based bioassays, we analyzed the binding of levamisole to the cocaine-binding DNA aptamer. At low aptamer concentrations ( 0.5 to 20 mu M) using isothermal titration calorimetry methods and thermal stability measurements, no binding of levamisole to the cocaine-binding aptamer was observed. At higher levamisole concentrations (500 mu M), weak binding to the cocaine-binding aptamer was detected using nuclear magnetic resonance (NMR) spectroscopy chemical shift perturbations. NMR-detected titrations show that levamisole binding is competitive with cocaine binding, indicating that both ligands share a common binding site. Finally, we show that the presence of levamisole does not interfere with the photochrome aptamer switch binding assay for cocaine. We conclude that assays using low concentrations of cocaine, and consequently low concentration of levamisole as an adulterant, should be unaffected by the weak binding of levamisole.
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页码:24209 / 24217
页数:9
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