Isolation and characterization of insulin in Russian sturgeon ( Acipenser guldenstaedti)

Insulin was isolated from the pancreas of Chondrostean fish, the Russian sturgeon, Acipenser guldenstaedti , by acid‐ethanol extraction followed by ion‐exchange and reverse‐phase high‐performance liquid chromatographies. The amino acid sequence determined by automated Edman degradation is as follows...

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Bibliographic Details
Published in:The Journal of Peptide Research
Main Authors: RUSAKOV, YU I., MORIYAMA, S., BONDAREVA, V. M., KOLYCHEV, A. P., AMEMIYA, Y., YASUDA, A., KAWAUCHI, H.
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1998
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Online Access:http://dx.doi.org/10.1111/j.1399-3011.1998.tb00637.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-3011.1998.tb00637.x
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-3011.1998.tb00637.x
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Summary:Insulin was isolated from the pancreas of Chondrostean fish, the Russian sturgeon, Acipenser guldenstaedti , by acid‐ethanol extraction followed by ion‐exchange and reverse‐phase high‐performance liquid chromatographies. The amino acid sequence determined by automated Edman degradation is as follows: A‐chain (21‐amino‐acid peptide), H‐Gly‐Ile‐Val‐Glu‐Gln‐Cys‐Cys‐His‐Ser‐Pro‐Cys‐Ser‐Leu‐Tyr‐Asp‐Leu‐Glu‐Asn‐Tyr‐Cys‐Asn‐OH; and B‐chain (31‐amino‐acid peptide), H‐Ala‐Ala‐Asn‐Gln‐His‐Leu‐Cys‐Gly‐Ser‐His‐Leu‐Val‐Glu‐Ala‐Leu‐Tyr‐Leu‐Val‐Cys‐Gly‐Glu‐Arg‐Gly‐Phe‐Phe‐Tyr‐Thr‐Pro‐Asn‐Lys‐Val‐OH. The sturgeon insulin appears to be identical with one of two forms of paddlefish insulin and differs from the other form by a single substitution in the A‐chain, Asp15: His15. The amino acid sequence of sturgeon insulin is more similar to the amino acid sequence of mammalian insulins than of other fish insulins. Sturgeon insulin showed parallel but weaker displacement than porcine insulin and pink salmon insulin in their respective radioimmunoassays and was less potent than porcine insulin in displacing radiolabeled porcine insulin bound to partially purified rat liver plasma membranes.