1,5-Diamino-2-pentyne is both a substrate and inactivator of
plant copper amine oxidases

J 2004

1,5-Diamino-2-pentyne is both a substrate and inactivator of plant copper amine oxidases

ŠEBELA, Marek, Zbyněk LAMPLOT, Michal MALOŇ, René LENOBEL, Karel LEMR et. al.

Základní údaje

Originální název

1,5-Diamino-2-pentyne is both a substrate and inactivator of plant copper amine oxidases

Autoři

ŠEBELA, Marek, Zbyněk LAMPLOT, Michal MALOŇ, René LENOBEL, Karel LEMR, Jan HAVLIŠ, Pavel PEČ, Chunhua QIAO a Lawrence M. SAYRE

Vydání

European Journal of Biochemistry, 2004, 0014-2956

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10600 1.6 Biological sciences

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 3.260

Organizační jednotka

Přírodovědecká fakulta

UT WoS

000225750800012

Klíčová slova anglicky

amine oxidase; diamine; mechanism-based inhibition; nuclear magnetic resonance; oxidation.

Štítky

amine oxidase, diamine, mechanism-based inhibition, nuclear magnetic resonance, oxidation.

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 2. 7. 2009 18:59, doc. Mgr. Jan Havliš, Dr.

Anotace

V originále

1,5-Diamino-2-pentyne (DAPY) was found to be a weak substrate of grass pea (Lathyrus sativus,GPAO) and sainfoin (Onobrychis viciifolia, OVAO) amine oxidases. Prolonged incubations, however, resulted in irreversible inhibition of both enzymes. For GPAO and OVAO, rates of inactivation of 0.10.3 min)1 were determined, the apparent KI values (half-maximal inactivation) were of the order of 10E-5 M. DAPY was found to be a mechanism-based inhibitor of the enzymes because the substrate cadaverine significantly prevented irreversible inhibition. The N1-methyl andN5-methyl analogs of DAPYwere tested with GPAO and were weaker inactivators (especially the N5-methyl) than DAPY. Prolonged incubations of GPAO or OVAO with DAPY resulted in the appearance of a yellowbrown chromophore (kmax = 310325 nm depending on the working buffer). Excitation at 310 nm was associated with emitted fluorescence with a maximum at 445 nm, suggestive of extended conjugation. After dialysis, the color intensity was substantially decreased, indicating the formation of a low molecular mass secondary product of turnover. The compound provided positive reactions with ninhydrin, 2-aminobenzaldehyde and Kovacs reagents, suggesting the presence of an amino group and a nitrogen-containing heterocyclic structure. The secondary product was separated chromatographically and was found not to irreversibly inhibit GPAO. MS indicated an exact molecular mass (177.14 Da) and molecular formula (C10H15N3). Electrospray ionization- and MALDI-MS/MS analyses yielded fragment mass patterns consistent with the structure of a dihydropyridine derivative of DAPY. Finally, N-(2,3-dihydropyridinyl)-1,5-diamino-2-pentyne was identified by means of 1H- and 13C-NMR experiments. This structure suggests a lysine modification chemistry that could be responsible for the observed inactivation.

Citovat

ŠEBELA, Marek, Zbyněk LAMPLOT, Michal MALOŇ, René LENOBEL, Karel LEMR, Jan HAVLIŠ, Pavel PEČ, Chunhua QIAO a Lawrence M. SAYRE. 1,5-Diamino-2-pentyne is both a substrate and inactivator of plant copper amine oxidases. European Journal of Biochemistry. 2004, č. 271, s. 4696-4708, 12 s. ISSN 0014-2956.

@article{567243,
   author = {Šebela, Marek and Lamplot, Zbyněk and Maloň, Michal and Lenobel, René and Lemr, Karel and Havliš, Jan and Peč, Pavel and Qiao, Chunhua and Sayre, Lawrence M.},
   article_number = {271},
   keywords = {amine oxidase; diamine; mechanism-based inhibition; nuclear magnetic resonance; oxidation.},
   language = {eng},
   issn = {0014-2956},
   journal = {European Journal of Biochemistry},
   title = {1,5-Diamino-2-pentyne is both a substrate and inactivator of plant copper amine oxidases},
   year = {2004}
}

TY  - JOUR
ID  - 567243
AU  - Šebela, Marek - Lamplot, Zbyněk - Maloň, Michal - Lenobel, René - Lemr, Karel - Havliš, Jan - Peč, Pavel - Qiao, Chunhua - Sayre, Lawrence M.
PY  - 2004
TI  - 1,5-Diamino-2-pentyne is both a substrate and inactivator of plant copper amine oxidases
JF  - European Journal of Biochemistry
IS  - 271
SP  - 4696-4708
EP  - 4696-4708
SN  - 00142956
KW  - amine oxidase
KW  - diamine
KW  - mechanism-based inhibition
KW  - nuclear magnetic resonance
KW  - oxidation.
N2  - 1,5-Diamino-2-pentyne (DAPY) was found to be a weak substrate of grass pea (Lathyrus sativus,GPAO) and sainfoin (Onobrychis viciifolia, OVAO) amine oxidases. Prolonged incubations, however, resulted in irreversible inhibition of both enzymes. For GPAO and OVAO, rates of inactivation of 0.10.3 min)1 were determined, the apparent KI values (half-maximal inactivation) were of the order of 10E-5 M. DAPY was found to be a mechanism-based inhibitor of the enzymes because the substrate cadaverine significantly prevented irreversible inhibition. The N1-methyl andN5-methyl analogs of DAPYwere tested with GPAO and were weaker inactivators (especially the N5-methyl) than DAPY. Prolonged incubations of GPAO or OVAO with DAPY resulted in the appearance of a yellowbrown chromophore (kmax = 310325 nm depending on the working buffer). Excitation at 310 nm was associated with emitted fluorescence with a maximum at 445 nm, suggestive of extended conjugation. After dialysis, the color intensity was substantially decreased, indicating the formation of a low molecular mass secondary product of turnover. The compound provided positive reactions with ninhydrin, 2-aminobenzaldehyde and Kovacs reagents, suggesting the presence of an amino group and a nitrogen-containing heterocyclic structure. The secondary product was separated chromatographically and was found not to irreversibly inhibit GPAO. MS indicated an exact molecular mass (177.14 Da) and molecular formula (C10H15N3). Electrospray ionization- and MALDI-MS/MS analyses yielded fragment mass patterns consistent with the structure of a dihydropyridine derivative of DAPY. Finally, N-(2,3-dihydropyridinyl)-1,5-diamino-2-pentyne was identified by means of 1H- and 13C-NMR experiments. This structure suggests a lysine modification chemistry that could be responsible for the observed inactivation.
ER  -

ŠEBELA, Marek, Zbyněk LAMPLOT, Michal MALOŇ, René LENOBEL, Karel LEMR, Jan HAVLIŠ, Pavel PEČ, Chunhua QIAO a Lawrence M. SAYRE. 1,5-Diamino-2-pentyne is both a substrate and inactivator of plant copper amine oxidases. \textit{European Journal of Biochemistry}. 2004, č.~271, s.~4696-4708, 12 s. ISSN~0014-2956.

Podrobný výpis o publikaci