Literature DB >> 24178481

Photophysical properties ofβ-homo-tyrosine derivatives.

L Lankiewicz1, J Lanoszka, S Ołdziej, W Wiczk.   

Abstract

The observed monoexponential fluorescence decay of N-acetyl-β-homo-tyrosine methylamide (Ac-βHty-NHMe) (I) and N-acetyl-(O-methyl)-β-homo-tyrosine methylamide (Ac-βHty(OMe)-NHMe) (II) is supporting the rotamer population theory, according to which rotamers are responsible for heterogeneity of the fluorescence decay of N-acetyl-tyrosine amide or tyrosine incorporated within a peptide chain, in general.

Year:  1996        PMID: 24178481     DOI: 10.1007/BF00806592

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  4 in total

1.  Rotamer-specific fluorescence quenching in tyrosinamide: Dynamic and static interactions.

Authors:  P B Contino; W R Laws
Journal:  J Fluoresc       Date:  1991-03       Impact factor: 2.217

2.  Pulsefluorimetry of tyrosyl peptides.

Authors:  P Gauduchon; P Wahl
Journal:  Biophys Chem       Date:  1978-03       Impact factor: 2.352

3.  Time-resolved fluorescence and 1H NMR studies of tyrosine and tyrosine analogues: correlation of NMR-determined rotamer populations and fluorescence kinetics.

Authors:  W R Laws; J B Ross; H R Wyssbrod; J M Beechem; L Brand; J C Sutherland
Journal:  Biochemistry       Date:  1986-02-11       Impact factor: 3.162

4.  Time-resolved fluorescence and 1H NMR studies of tyrosyl residues in oxytocin and small peptides: correlation of NMR-determined conformations of tyrosyl residues and fluorescence decay kinetics.

Authors:  J B Ross; W R Laws; A Buku; J C Sutherland; H R Wyssbrod
Journal:  Biochemistry       Date:  1986-02-11       Impact factor: 3.162

  4 in total

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