RESUMEN
Favourable analytical conditions allowing amino acid analysis in biological fluids, acquired from small human biopsy specimens, were achieved by considering various derivatization methods, the mode of detection and the column used. By using o-phthalaldehyde-3-mercaptopropionic acid as derivatization agent (high sensitivity and stability) and fluorescence detection (excitation at 330 nm, emission at 450 nm), excellent separation of 26 amino acids was obtained in the lower pmol range (1-10 pmol). The reproducibility of the retention times was better than 1.0% for the majority of amino acids and the results from high-performance liquid chromatography (HPLC), compared favourably with those of conventional amino acid analysis (r = 0.97). HPLC technology facilitates amino acid analysis in biopsy specimens of less than 1 mg of tissue.
Asunto(s)
Aminoácidos/análisis , Líquidos Corporales/análisis , Ácido 3-Mercaptopropiónico , Adulto , Cromatografía Líquida de Alta Presión , Humanos , Hígado/análisis , Masculino , Músculos/análisis , Espectrometría de Fluorescencia , Espectrofotometría Ultravioleta , o-FtalaldehídoAsunto(s)
Proteínas en la Dieta/efectos adversos , Manipulación de Alimentos , Lisina/análogos & derivados , Lisinoalanina/efectos adversos , Animales , Fenómenos Químicos , Química , Culinaria , Humanos , Riñón/patología , Enfermedades Renales/inducido químicamente , Enfermedades Renales/patología , Lisinoalanina/síntesis química , Lisinoalanina/toxicidad , Ratas , Terminología como AsuntoRESUMEN
Lysine peptides, X-Lys-OH (Formula: see text) were synthesized, following classic or non-classic routes. Some bacterial and mammalian enzymes, endo- and exo-peptide hydrolases of the enzyme nomenclature type EC 3.4., were tested for their ability to split the epsilon-peptide bond in the above substrates. Kinetic constants (Km,kcat) were evaluated with leucine aminopeptidase from hog kidney and eye lens with aminopeptidase I from yeast. Aminopeptidase M (hog pancreas) and hog intestinal aminopeptidase were additionally examined for their Ki values with the above substrates in comparison to the classic protease substrate leucine p-nitroanilide. Especially the intestinal mucosa hydrolases are shown to be efficient in cleaving epsilon-peptide bonds.
Asunto(s)
Oligopéptidos/síntesis química , Péptido Hidrolasas/metabolismo , Secuencia de Aminoácidos , Animales , Endopeptidasas/metabolismo , Glicina , Riñón/enzimología , Cinética , Cristalino/enzimología , Leucil Aminopeptidasa/metabolismo , Lisina , Fenilalanina , Saccharomyces cerevisiae/enzimología , Relación Estructura-Actividad , Especificidad por Sustrato , PorcinosAsunto(s)
Aminoácidos Esenciales/administración & dosificación , Proteínas en la Dieta , Proteínas de la Leche , Péptidos , Animales , Estudios de Evaluación como Asunto , Isoleucina/administración & dosificación , Metionina/administración & dosificación , Fenilalanina/administración & dosificación , Ratas , Tirosina/administración & dosificaciónRESUMEN
(Aminoacyl)n=1-10-AH-Sepharoses can easily be prepared by the N-carboxy anhydride method from amino acid N-carboxy anhydrides and AH-Sepharose 4B at pH 10.2, 0degreesC in aqueous borate buffer. Syntheses of cystinyl-, cysteinyl-, isoleucyl-, leucyl- and phenylalanyl-AH-Sepharoses are described. An improved preparation for cystine bis(N-carboxy anhydride) is presented.