Targeting the human serotonin transporter (hSERT) with quantum dots

被引:0
|
作者
Tomlinson, I. D. [1 ]
Chang, Jerry [1 ]
Iwamoto, Hideki [2 ]
De Felice, Louis J. [2 ,3 ]
Blakely, Randy D. [2 ,3 ]
Rosenthal, Sandra J. [1 ,2 ]
机构
[1] Vanderbilt Univ, Dept Chem, Stn B 311822, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Ctr Mol Neurosci, Nashville, TN 37232 USA
关键词
quantum dots; serotonin; hSERT; antagonist; paroxetine;
D O I
10.1117/12.782801
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this paper we report our work on the development of a human serotonin transporter (hSERT) antagonist that can be conjugated to quantum dots. This approach has been used to target and visualize the human serotonin transporter protein (hSERT). We demonstrate that labeling is blocked by the addition of high affinity hSERT antagonists such as paroxetine. This approach may be useful for the development of fluorescent assays to study the location and temporal dynamics of biogenic amine transporters and also holds promise for the development of plate-based high throughput assays used to identify novel transporter antagonists.
引用
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页数:12
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