Literature DB >> 1880193

Chromatographic and physical studies of tropomyosin in aqueous-organic media at low pH.

D L Crimmins1, M E Holtzer.   

Abstract

Non-cross-linked and disulfide-cross-linked two-chain molecules comprising the alpha and/or beta chains of rabbit skeletal tropomyosin were studied by electrophoretic, chromatographic and physical methods. Elution order on C4 reversed-phase high-performance liquid chromatography depends markedly on the number and position of the cross-links. In the C4 reversed-phase elution medium, cross-linked and non-cross-linked species are greater than 85% helical by circular dichroism, but the non-cross-linked elute later from high-performance size-exclusion chromatography (G4000) and have molecular mass of 31,000-41,000 dalton by equilibrium ultracentrifugation. The data suggest that in the C4 reversed-phase high-performance liquid chromatography elution medium non-cross-linked tropomyosin exists as amphipathic single-chain alpha-helices.

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Year:  1991        PMID: 1880193     DOI: 10.1016/s0021-9673(01)95785-1

Source DB:  PubMed          Journal:  J Chromatogr


  2 in total

1.  Rapid, spontaneous reassembly of homo- and heterodimeric tropomyosin two-chain coiled coils from unfolded single alpha and beta chains.

Authors:  J Mo; M E Holtzer; A Holtzer
Journal:  Protein Sci       Date:  1993-01       Impact factor: 6.725

2.  Beta beta homodimers exist in native rabbit skeletal muscle tropomyosin and increase after denaturation-renaturation.

Authors:  M E Holtzer; S G Kidd; D L Crimmins; A Holtzer
Journal:  Protein Sci       Date:  1992-03       Impact factor: 6.725

  2 in total

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