http://www.cnr.it/ontology/cnr/individuo/prodotto/ID12715
Identification by site-directed mutagenesis and chemical modification of three vicinal cysteine residues in rat mitochondrial carnitine/acylcarnitine transporter (Articolo in rivista)
- Type
- Label
- Identification by site-directed mutagenesis and chemical modification of three vicinal cysteine residues in rat mitochondrial carnitine/acylcarnitine transporter (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Tonazzi A; Giangregorio N; Indiveri C; Palmieri F. (literal)
- Pagina inizio
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- National Research Council Institute of Biomembranes and Bioenergetics (IBBE), via Amendola 165/A, 70126, Bari, Italy
Department of Cellular Biology, University of Calabria, Via P.Bucci cubo 4c, 87036 Arcavacata di Rende (CS), Italy
Laboratory of Biochemistry and Molecular Biology, Department of Pharmaco-Biology, University of Bari, Via Orabona 4, 70125 Bari, Italy (literal)
- Titolo
- Identification by site-directed mutagenesis and chemical modification of three vicinal cysteine residues in rat mitochondrial carnitine/acylcarnitine transporter (literal)
- Abstract
- The proximity of the Cys residues present in the mitochondrial rat
carnitine/acylcarnitine carrier (CAC) primary structure was studied by
using site-directed mutagenesis in combination with chemical
modification. CAC mutants, in which one or more Cys residues had been
replaced with Ser, were overexpressed in E.coli and reconstituted into
liposomes. The effect of SH oxidizing, cross-linking and coordinating
reagents was evaluated on the carnitine/carnitine exchange catalyzed by
the recombinant reconstituted CAC proteins. All the reagents tested
efficiently inhibited the wild-type CAC. The inhibitory effect of diamide,
Cu2+-phenanthroline or phenylarsine oxide was largely reduced or
abolished by the double substitutions C136/155S, C58/136S and
C58/155S. The decrease in sensitivity to these reagents was much lower
in double mutants in which Cys-23 was substituted with Cys-136 or Cys-
155. No decrease in inhibition was found when Cys-89 and/or Cys-283
were replaced with Ser. Sb3+, which coordinates three cysteines, inhibited
only the Cys-replacement mutants containing all three cysteines 58, 136
and 155 out of the six native cysteines. In addition, the mutant
C23/89/155/283S, in which double tandem fXa recognition sites were
inserted in position 65-72, i.e. between Cys-58 and Cys-136, was not
cleaved into two fragments by fXa protease after treatment with diamide.
These results are interpreted in the light of the homology model of CAC
based on the available X-ray structure of the ADP/ATP carrier. They
indicate that Cys-58, Cys-136 and Cys-155 become close in the tertiary
structure of the CAC during its catalytic cycle. (literal)
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