Reversible binding interactions between the tryptophan enantiomers and albumins of different animal species as determined by novel high performance liquid chromatographic methods: An attempt to localize the D- and L- tryptophan binding sites on the human serum albumin polypeptide chain by using protein fragments

Chirality

Volumn 9, Issue 4, 1997, Pages 373-379

  Šoltés, Ladislav ^a   Sebille, Bernard ^b  

^a INSTITUTE OF EXPERIMENTAL PHARMACOLOGY AND TOXICOLOGY   (Slovakia)

^b UNIVERSITÉ PARIS EST CRÉTEIL   (France)

Author keywords

BSA HSA bond silica gel; Chiral separation; Column switching; Enantioselectivity; High performance liquid chromatography; Hummel and Dreyer method; Polarimetric chiroptical detection; Protein drug binding

Indexed keywords

ALBUMIN; TRYPTOPHAN;

ARTICLE; BINDING SITE; CHIRALITY; DRUG PROTEIN BINDING; ENANTIOMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; POLARIMETRY; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; STEREOCHEMISTRY; ULTRAVIOLET SPECTROPHOTOMETRY;

EID: 1842338655     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1520-636x(1997)9:4<373::aid-chir10>3.3.co;2-9     Document Type: Article

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