Kasinathan C, Xu Z C, Kirchberger M A
Department of Physiology and Biophysics, Mount Sinai School of Medicine, City University of New York, New York 10029.
Biochem Biophys Res Commun. 1988 Dec 30;157(3):1296-301. doi: 10.1016/s0006-291x(88)81015-5.
Phospholamban (PLM) is detectable by Western blot analysis of canine cardiac microsomes using rabbit antiserum against a peptide containing the 2 to 30 amino acid sequence of PLM. Phosphorylated PLM is distinguishable from the unphosphorylated form by virtue of a reduced electrophoretic mobility. Utilizing digital image analysis to determine relative band densities, it was found that the ratio of unphosphorylated to phosphorylated PLM is correlated with the rate of calcium uptake in 5 preparations of native microsomes (r = 0.94, p less than 0.01). The present analysis may be useful for determining the phosphorylation state of PLM in microsomes obtained from animals in physiological states characterized by impaired sarcoplasmic reticulum calcium pump activity.
使用针对包含磷蛋白(PLM)第2至30个氨基酸序列的肽段的兔抗血清,通过蛋白质免疫印迹分析犬心脏微粒体可检测到PLM。磷酸化的PLM因其电泳迁移率降低而与未磷酸化形式相区分。利用数字图像分析来确定相对条带密度,发现在5份天然微粒体制剂中,未磷酸化与磷酸化PLM的比率与钙摄取速率相关(r = 0.94,p小于0.01)。本分析对于确定从肌浆网钙泵活性受损的生理状态动物获得的微粒体中PLM的磷酸化状态可能有用。