| Literature DB >> 7000657 |
W Danho, A Sasaki, E Büllesbach, H G Gattner, A Wollmer.
Abstract
An analogue of porcine insulin which differs from the native molecule in that the amino acid residue A14-tyrosine is replaced by phenylalanine has been synthesized. The [PheA14]A chain was synthesized by the fragment condensation method and purified as tetra-S-sulfonate by ion-exchange chromatography on DEAE-cellulose at pH 5.6. Conversion of the tetra-S-sulfonate A chain to the sulfhydryl form and combination with native porcine sulfhydryl B chain gave the [PheA14]insulin, which was purified by gel filtration and ion-exchange chromatography on DEAE-cellulose. The biological activity of this analogue was 96 +/- 6% as measured by the rat epididymal adipocytes. This shows that A14-tyrosine is not essential for the biological activity of the hormone.Entities:
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Year: 1980 PMID: 7000657 DOI: 10.1515/bchm2.1980.361.1.747
Source DB: PubMed Journal: Hoppe Seylers Z Physiol Chem ISSN: 0018-4888