Quantitative Detection of μ Opioid Receptor: Western Blot Analyses Using μ Opioid Receptor Knockout Mice

被引:10
|
作者
Kasai, Shinya
Yamamoto, Hideko
Kamegaya, Etsuko
Uhl, George R. [2 ]
Sora, Ichiro [3 ]
Watanabe, Masahiko [4 ]
Ikeda, Kazutaka [1 ]
机构
[1] Tokyo Inst Psychiat, Div Psychobiol, Setagaya Ku, Tokyo 1568585, Japan
[2] Natl Inst Drug Abuse, Mol Neurobiol Branch, NIH, Bethesda, MD 21224 USA
[3] Tohoku Univ, Grad Sch Med, Dept Neurosci, Div Psychobiol, Sendai, Miyagi 9808574, Japan
[4] Hokkaido Univ, Grad Sch Med, Dept Anat & Embryol, Sapporo, Hokkaido 0608638, Japan
基金
美国国家卫生研究院;
关键词
Knockout mice; mu opioid receptor; quantification; Western blot analysis; POSITRON-EMISSION-TOMOGRAPHY; MESSENGER-RNA LEVELS; COCAINE TREATMENT; BRAIN; EXPRESSION; DEPENDENCE; OPIATE; DELTA;
D O I
10.2174/157015911795016921
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Increasing evidence suggests that mu opioid receptor (MOP) expression is altered during the development of and withdrawal from substance dependence. Although anti-MOP antibodies have been hypothesized to be useful for estimating MOP expression levels, inconsistent MOP molecular weights (MWs) have been reported in studies using anti-MOP antibodies. In the present study, we generated a new anti-MOP antibody (N38) against the 1-38 amino acid sequence of the mouse MOP N-terminus and conducted Western blot analysis with wildtype and MOP knockout brain lysates to determine the MWs of intrinsic MOP. The N38 antibody detected migrating bands with relative MWs of 60-67 kDa in the plasma membrane fraction isolated from wildtype brain, but not from the MOP knockout brain. These migrating bands exhibited semi-linear density in the range of 3-30 mu g membrane proteins/lane. The N38 antibody may be useful for quantitatively detecting MOP.
引用
收藏
页码:219 / 222
页数:4
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