Pregled bibliografske jedinice broj: 531882
Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3
Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3 // European journal of human genetics, 15 (2007), 3; 347-351 doi:10.1038/sj.ejhg.5201757 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 531882 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3
Autori
Fumić, Ksenija ; Belužić, Robert ; Ćuk, Mario ; Pavkov, Tea ; Kloor, Doris ; Barić, Ivo ; Mijić, Ivana ; Vugrek, Oliver
Izvornik
European journal of human genetics (1018-4813) 15
(2007), 3;
347-351
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
AdoHcyase; recombinant protein; thermo sensitivity; circular dichroism; vascular disease
Sažetak
S-adenosylhomocysteine hydrolase (AdoHcyase) catalyzes the hydrolysis of AdoHcy to adenosine and homocysteine. Increased levels of AdoHcy may play a role in the development of cardiovascular diseases and numerous other conditions associated with hyperhomocysteinemia. Several polymorphic isoforms named SAHH-1 to 4 may be resolved by horizontal starch gel electrophoresis from red blood cells. We have identified the genetic background of isoforms SAHH-2 and SAHH-3. SAHH-2 represents the previously described polymorphism in exon 2 of the AdoHcyase gene (112 C>T ; p.R38W). Isoform SAHH-3 is based on a new polymorphism in exon 3 (377 G>A), leading to the conversion of glycine to arginine at amino-acid position 123. To shed light on the effects of these polymorphisms on the molecular and catalytic properties of AdoHcyase, we made recombinant wild-type and polymorphic R38W and G123R enzymes for a comparative analysis. The amino-acid exchanges did not bring about major changes to the catalytic rates of the recombinant proteins. However, circular dichroism analysis showed that both polymorphisms effect the thermal stability of the recombinant protein in vitro, reducing the unfolding temperature by approximately 2.6°C (R38W) and 1.5°C (G123R) compared to wild-type protein. In view of the altered thermal stability, and slightly decreased enzymatic activity of polymorphic proteins (less than or equal to6%), one may consider the analyzed AdoHcyase isoforms as risk markers for diseases caused by irregular AdoHcyase metabolism.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Klinički bolnički centar Zagreb
Profili:
Ivo Barić
(autor)
Ksenija Fumić
(autor)
Robert Belužić
(autor)
Ivana Dodig
(autor)
Oliver Vugrek
(autor)
Ivana Mijić
(autor)
Mario Ćuk
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE