Targeted proteomics of cannabinoid receptor CB1 and the CB1b isoform

被引:7
|
作者
Ghosh, Soumita [1 ]
Gonzalez-Mariscal, Isabel [1 ]
Egan, Josephine M. [1 ]
Moaddel, Ruin [1 ]
机构
[1] NIA, Biomed Res Ctr, NIH, 251 Bayview Blvd, Baltimore, MD 21224 USA
关键词
CB1; CB1b; Cannabinoid receptor isoforms; SRM assay; BETA-CELLS; INSULIN-SECRETION; GPR55; METABOLISM; PANCREAS; VARIANT; ISLETS; MICE;
D O I
10.1016/j.jpba.2016.11.003
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Cannabinoid receptors (CBR), including CB1 and CB2 have been therapeutic targets for a number of conditions. Recently, splice variants of the CB1R have been identified in humans. The isoforms differ in their N-terminus sequence and pharmacological activity relative to the CB1R, as a result, the differentiation between the CB1 receptor and its isoform is required. As a result, a selected reaction monitoring mass spectrometry (SRM-MS) method was developed for the quantitation of CB1 and the CB1 b isoform in CHO cells transduced with CB1 and CB1b. The SRM-MS protocol was assessed with isotopically labeled peptide standards and had high reproducibility of intra-day assay (CVs from 1.9 to 4.3% for CB1 and 0.5 to 5.9% for CB1b) and inter-day assay (CVs from 1.2 to 5.2% for CBI and 1.2 to 6.1% for CB1b). Published by Elsevier B.V.
引用
收藏
页码:154 / 158
页数:5
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