Synthesis of CCK-8 tetrapeptide fragment by enzymatic method

Xiang Guangya , Heiner Eckstein

Current Medical Science ›› 2003, Vol. 23 ›› Issue (7) : 234 -235.

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Current Medical Science ›› 2003, Vol. 23 ›› Issue (7) : 234 -235. DOI: 10.1007/BF02829500
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Synthesis of CCK-8 tetrapeptide fragment by enzymatic method

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Abstract

The enzymatic synthesis of a tetrapeptide Phac-Met-Gly-Trp-Met-OEt, a fragment of the cholecystokinin C-terminal octapeptide CCK-8, was reported. This fragment was synthesized by coupling Phac-Met-OEt with Gly-OMe, Trp-OMe and Met-OEf successively. These three steps were catalyzed by α-chymotrpsin, Papain and α-chymotrpsin respectively. The results of FAB-MS showed that all the products had the correct molecular mass.

Keywords

CCK-8 / enzymatic method / α-chymotrpsin / papain

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Xiang Guangya, Heiner Eckstein. Synthesis of CCK-8 tetrapeptide fragment by enzymatic method. Current Medical Science, 2003, 23(7): 234-235 DOI:10.1007/BF02829500

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References

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EcksteinH, HuettnerD, LuZ M. MarinezJean, FehrentzJean-Alain. Synthesis of the cholecystokinin peptide CCK-4 exclusively by enzymatic methods. Peptides 2000, 2001, Paris, France, EDK: 329-330

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KullmanW. Protease-catalyzed peptide bone formation: Application to synthesis of the COOH-terminal octapeptide of cholecystokinin. Proc Natl Acad Sci (USA), 1982, 79: 2840-2840

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CalvetS, TorresJ L, ClapesP. Enzymatic peptide synthesis in organic media. Synthesis of CCK-8 dipeptide fragments. Biocataly Biotransform, 1996, 13: 201-201

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CapellasM, BenaigesM D, CaminalG, et al.. Enzymatic synthesis of a CCK-8 tripeptide fragment in organic media. Biotechnol Bioeng, 1996, 50: 700-700

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