Balagopal P, Nair K S, Stirewalt W S
Department of Medicine, Endocrinology and Metabolism, University of Vermont, Burlington 05405.
Anal Biochem. 1994 Aug 15;221(1):72-7. doi: 10.1006/abio.1994.1381.
A convenient procedure for the isolation of milligram quantities of myosin heavy chain (MHC) from small samples of muscle tissue using preparative gel electrophoresis is described. Application of the methodology to measurements of the fractional synthesis rates (ks) of MHC using skeletal muscle biopsy samples from humans and cardiac tissue from pigs following continuous intravenous infusions of stable isotope (L-[1-13C]-leucine) is demonstrated. The sensitivity and reproducibility of the determination of stable isotope enrichment are also defined. In addition, measurements of the ks of MHC in skeletal muscle of rats in vivo using radioisotope-tracer methodologies are described.
描述了一种使用制备性凝胶电泳从小块肌肉组织样本中分离毫克量肌球蛋白重链(MHC)的简便方法。展示了将该方法应用于通过连续静脉输注稳定同位素(L-[1-13C]-亮氨酸)后,对来自人类的骨骼肌活检样本和猪的心脏组织进行MHC的分数合成率(ks)测量。还定义了稳定同位素富集测定的灵敏度和重现性。此外,描述了使用放射性同位素示踪方法在体内测量大鼠骨骼肌中MHC的ks。