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用于Trk受体酪氨酸激酶调节剂高通量筛选的细胞分析方法。

Cellular assays for high-throughput screening for modulators of Trk receptor tyrosine kinases.

作者信息

Wang Jun, Hancock Michael K, Dudek Jeanne M, Bi Kun

机构信息

Invitrogen Corporation, Discovery Sciences, 501 Charmany Drive, Madison, WI 53719, USA.

出版信息

Curr Chem Genomics. 2008 Feb 25;1:27-33. doi: 10.2174/1875397300801010027.

Abstract

Trk receptor tyrosine kinases are required for signal transduction initiated by neurotrophins leading to cell proliferation, differentiation, survival and death. Alterations in Trk kinase activity have been linked to various diseases. To address the need for cell-based assays for screening and studying the selectivity of Trk kinase modulators, we developed high-throughput cell-based assays for Trk receptor kinases using nuclear factor of activated T-cells (NFAT) beta-lactamase reporter lines stably expressing full length human Trk kinases. These assays were functionally validated with cognate neurotrophin(s), inhibitors and TRK RNAi oligos and demonstrated for their utility in identifying potent and selective modulators of Trk receptor kinases.

摘要

Trk受体酪氨酸激酶是神经营养因子启动信号转导所必需的,该信号转导导致细胞增殖、分化、存活和死亡。Trk激酶活性的改变与多种疾病有关。为了满足基于细胞的检测方法用于筛选和研究Trk激酶调节剂选择性的需求,我们利用稳定表达全长人Trk激酶的活化T细胞核因子(NFAT)β-内酰胺酶报告细胞系,开发了用于Trk受体激酶的高通量细胞检测方法。这些检测方法通过同源神经营养因子、抑制剂和TRK RNAi寡核苷酸进行了功能验证,并证明了其在鉴定Trk受体激酶的有效和选择性调节剂方面的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6443/2774616/acec97e7df35/TOCHGENJ-1-27_F1.jpg

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