Non-invasive single cell aptasensing in live cells and animals

被引:0
|
作者
Osman, Eiman A. [1 ]
Rynes, Thomas P. [2 ]
Wang, Y. Lucia [3 ]
Mruk, Karen [2 ]
Mckeague, Maureen [1 ,3 ]
机构
[1] McGill Univ, Fac Sci, Dept Chem, Montreal, PQ H3A 0B8, Canada
[2] East Carolina Univ, Brody Sch Med, Dept Pharmacol & Toxicol, Greenville, NC 27834 USA
[3] McGill Univ, Fac Med & Hlth Sci, Pharmacol & Therapeut, Montreal, PQ H3G 1Y6, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
GREEN FLUORESCENT PROTEIN; GENETICALLY-ENCODED BIOSENSORS; GENE-EXPRESSION; IN-VIVO; RNA; SELECTION; TOXICITY; DESIGN;
D O I
10.1039/d3sc05735f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report a genetically encoded aptamer biosensor platform for non-invasive measurement of drug distribution in cells and animals. We combined the high specificity of aptamer molecular recognition with the easy-to-detect properties of fluorescent proteins. We generated six encoded aptasensors, showcasing the platform versatility. The biosensors display high sensitivity and specificity for detecting their specific drug target over related analogs. We show dose dependent response of biosensor performance reaching saturating drug uptake levels in individual live cells. We designed our platform for integration into animal genomes; thus, we incorporated aptamer biosensors into zebrafish, an important model vertebrate. The biosensors enabled non-invasive drug biodistribution imaging in whole animals across different timepoints. To our knowledge, this is the first example of an aptamer biosensor-expressing transgenic vertebrate that is carried through generations. As such, our encoded platform addresses the need for non-invasive whole animal biosensing ideal for pharmacokinetic-pharmacodynamic analyses that can be expanded to other organisms and to detect diverse molecules of interest. A genetically encoded aptasensor platform for non-invasive measurement of drug distribution in cells and zebrafish was developed.
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页数:10
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