Literature DB >> 7470053

Incorporation of amino acids into soluble and membrane protein fractions of dystrophic hamsters.

D M Nicholls, R C Creasy, M W Chin-See, J A Carlisle, A B Lange, M Saleem.   

Abstract

The incorporation of labelled leucine was measured in protein fractions of muscle in intact control and dystrophic female hamsters and also in cell-free preparations obtained from these animals. The labelling of the soluble sarcoplasmic protein fraction, the microsomal protein fraction and the sarcolemma protein fraction was increased in the dystrophic hindleg muscle. The specific radioactivities of the sarcolemma protein fraction and other fractions were increased markedly relative to that of free leucine in the dystrophic muscle. In cell-free preparations where ribonuclease effects were avoided, the dystrophic muscle exhibited an increased synthesis of peptide bonds.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 7470053      PMCID: PMC1162099          DOI: 10.1042/bj1900341

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  44 in total

1.  Ca-2+ transport and assembly of protein particles in sarcoplasmic membranes isolated from normal and dystrophic muscle.

Authors:  R Sabbadini; D Scales; G Inesi
Journal:  FEBS Lett       Date:  1975-06-01       Impact factor: 4.124

2.  Skeletal-muscle growth and protein turnover.

Authors:  D J Millward; P J Garlick; R J Stewart; D O Nnanyelugo; J C Waterlow
Journal:  Biochem J       Date:  1975-08       Impact factor: 3.857

3.  The relative importance of muscle protein synthesis and breakdown in the regulation of muscle mass.

Authors:  D J Millward; P J Garlick; D O Nnanyelugo; J C Waterlow
Journal:  Biochem J       Date:  1976-04-15       Impact factor: 3.857

4.  The effects of denervation on protein turnover of rat skeletal muscle.

Authors:  D F Goldspink
Journal:  Biochem J       Date:  1976-04-15       Impact factor: 3.857

5.  Protein synthesis in dystrophic muscle. Activity of the pH 5 supernatant fraction of muscle in dystrophic mice.

Authors:  R Petryshyn; D M Nicholls
Journal:  Biochim Biophys Acta       Date:  1976-07-16

6.  Protein and RNA synthesis in the skeletal muscle of hereditary dystrophic mouse.

Authors:  Y Hayashi; H O Suzuki; T Totsuka
Journal:  J Biochem       Date:  1975-04       Impact factor: 3.387

7.  Defective membrane systems in dystrophic skeletal muscle of the UM-X7.1 strain of genetically myopathic hamster.

Authors:  N S Dhalla; A Singh; S L Lee; M B Anand; A M Bernatsky; G Jasmin
Journal:  Clin Sci Mol Med       Date:  1975-10

8.  Activity of polyribosomes from the muscle of normal and dystrophic mice in cell-free amino-acid incorporation.

Authors:  M Nwagwu
Journal:  Eur J Biochem       Date:  1975-08-01

9.  Biochemical abnormalities of erythrocyte membranes in Duchenne dystrophy. Adenosine triphosphatase and adenyl cyclase.

Authors:  S Mawatari; M Schonberg; M Olarte
Journal:  Arch Neurol       Date:  1976-07

10.  Characterization of the adenosinetriphosphatase and calsequestrin isolated from sarcoplasmic reticulum of normal and dystrophic chickens.

Authors:  J L YAP; D H MacLennan
Journal:  Can J Biochem       Date:  1976-07
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.