Analogues of trypsin inhibitor SFTI-1 modified in the conserved P1′ position by synthetic or non-proteinogenic amino acids retain their inhibitory activity - Publication - Bridge of Knowledge

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Analogues of trypsin inhibitor SFTI-1 modified in the conserved P1′ position by synthetic or non-proteinogenic amino acids retain their inhibitory activity

Abstract

A series of linear and monocyclic (with a disulfide bridge only) analogues of trypsin inhibitor SFTI-1 modified in the P-1 and/or P-1' positions were synthesized by the solid-phase method. In the substrate specificity P-1 position, Phe or N-benzylglycine (Nphe) were introduced, whereas the conserved Ser6 in Bownam-Birk (BBI) inhibitors was replaced by Hse (L-homoserine), Nhse [N-(2-hydroxyethyl)glycine], Sar, and Ala. Kinetic studies of interaction of the analogues with bovine alpha-chymotrypsin have shown that in monocyclic (but not linear) analogues, Hse and Nhse are tolerated to afford potent inhibitors. This is the first evidence that the absolutely conserved Ser present in the inhibitor's P-1' position can be successfully replaced by a synthetic derivative. Copyright (C) 2011 European Peptide Society and John Wiley & Sons, Ltd.

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Authors (7)

  • Photo of  Łukajtis Rafał

    Łukajtis Rafał

    • University of Gdansk
  • Photo of  Łȩgowska Anna

    Łȩgowska Anna

    • University of Gdansk
  • Photo of  Wysocka Magdalena

    Wysocka Magdalena

    • University of Gdansk
  • Photo of  Dȩbowski Dawid

    Dȩbowski Dawid

    • University of Gdansk
  • Photo of  Lesner Adam

    Lesner Adam

    • University of Gdansk
  • Photo of  Rolka Krzysztof

    Rolka Krzysztof

    • University of Gdansk

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Accepted or Published Version
DOI:
Digital Object Identifier (open in new tab) 10.1002/psc.1330
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Copyright (2011 European Peptide Society and John Wiley & Sons, Ltd)

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Details

Category:
Articles
Type:
artykuł w czasopiśmie wyróżnionym w JCR
Published in:
JOURNAL OF PEPTIDE SCIENCE no. 17, edition 4, pages 281 - 287,
ISSN: 1075-2617
Language:
English
Publication year:
2011
Bibliographic description:
Rafał Ł., Anna Ł., Magdalena W., Dawid D., Adam L., Krzysztof R.: Analogues of trypsin inhibitor SFTI-1 modified in the conserved P1′ position by synthetic or non-proteinogenic amino acids retain their inhibitory activity// JOURNAL OF PEPTIDE SCIENCE. -Vol. 17, iss. 4 (2011), s.281-287
DOI:
Digital Object Identifier (open in new tab) 10.1002/psc.1330
Verified by:
Gdańsk University of Technology

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