Subcellular sorting of isoactins: Selective association of γ actin with skeletal muscle mitochondria
Cell, ISSN: 0092-8674, Vol: 32, Issue: 4, Page: 1093-1103
1983
- 78Citations
- 21Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations78
- Citation Indexes78
- 78
- CrossRef67
- Captures21
- Readers21
- 21
Article Description
We describe two subpopulations of actin antibodies isolated by affinity chromatography from a polyclonal antibody to chicken gizzard actin. One subpopulation recognizes γ actins from smooth muscle and nonmuscle cells, but does not recognize α actin from skeletal muscle. The other subpopulation recognizes determinants that are common to a actin from skeletal muscle and the two γ actin isotypes. Neither antibody recognizes cytoplasmic β actin. Both antibodies recognize only actins or molecules with determinants that are also present in actins. By immunofluorescence we found that the anti-γ actin colocalizes with mitochondria in fibers of mouse diaphragm, and that it does not bind detectably to the I bands of sarcomeres. The antibody that recognizes both α and γ actins stains I bands intensely, as expected. We interpret these observations as preliminary evidence for selective association of γ actin with skeletal muscle mitochondria and, more broadly, as evidence for subcellular sorting of isoactins.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/0092867483902933; http://dx.doi.org/10.1016/0092-8674(83)90293-3; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0020967398&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/6340835; https://linkinghub.elsevier.com/retrieve/pii/0092867483902933; http://dx.doi.org/10.1016/0092-8674%2883%2990293-3; https://dx.doi.org/10.1016/0092-8674%2883%2990293-3
Elsevier BV
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