Is there Any Correlation Between Binding and Functional Effects at the Translocator Protein (TSPO) (18 kDa)?

被引:3
|
作者
Scarf, A. M. [1 ,2 ,3 ]
Auman, K. M. [1 ,2 ,4 ]
Kassiou, M. [1 ,2 ,4 ]
机构
[1] Univ Sydney, Brain & Mind Res Inst, Drug Discovery Lab, Camperdown, NSW 2050, Australia
[2] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[3] Univ Sydney, Discipline Pharmacol, Sydney, NSW 2006, Australia
[4] Univ Sydney, Discipline Med Radiat Sci, Sydney, NSW 2006, Australia
关键词
Apoptosis; multiple binding sites; neuroprotection; radioligand binding; steroidogenesis; translocator protein (TSPO); PERIPHERAL BENZODIAZEPINE-RECEPTOR; HUMAN BREAST-CANCER; ACUTE REGULATORY PROTEIN; DEPENDENT ANION CHANNEL; TUMOR-NECROSIS-FACTOR; CELL-CYCLE ARREST; H-3; PK; 11195; MICROGLIAL ACTIVATION; IN-VIVO; HIGH-AFFINITY;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The translocator protein (TSPO) is a potential drug target for the treatment of CNS diseases, with TSPO ligands being able to modulate steroidogenesis, apoptosis, and cell proliferation. While there exist multiple TSPO binding sites, the nature of these sites - either overlapping or allosterically linked - remains largely uncharacterized. Furthermore, while evidence suggests that microglial activation and polymerization result in changes to TSPO binding sites, these changes are poorly understood. While current pharmacophoric models can be used to synthesize TSPO ligands with high affinity and selectivity, these models are unable to predict ligands with desirable functional effects. Better characterization of TSPO binding sites in health and disease may provide insight into particular sites which mediate promising therapeutic profiles, thus refining the TSPO pharmacophore.
引用
收藏
页码:387 / 397
页数:11
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