Pretražite po imenu i prezimenu autora, mentora, urednika, prevoditelja

Napredna pretraga

Pregled bibliografske jedinice broj: 531882

Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3


Fumić, Ksenija; Belužić, Robert; Ćuk, Mario; Pavkov, Tea; Kloor, Doris; Barić, Ivo; Mijić, Ivana; Vugrek, Oliver
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:

Avatar Url Ivo Barić (autor)

Avatar Url Ksenija Fumić (autor)

Avatar Url Robert Belužić (autor)

Avatar Url Ivana Dodig (autor)

Avatar Url Oliver Vugrek (autor)

Avatar Url Ivana Mijić (autor)

Avatar Url Mario Ćuk (autor)

Citiraj ovu publikaciju:

Fumić, Ksenija; Belužić, Robert; Ćuk, Mario; Pavkov, Tea; Kloor, Doris; Barić, Ivo; Mijić, Ivana; Vugrek, Oliver
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)
Fumić, K., Belužić, R., Ćuk, M., Pavkov, T., Kloor, D., Barić, I., Mijić, I. & Vugrek, O. (2007) Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3. European journal of human genetics, 15 (3), 347-351 doi:10.1038/sj.ejhg.5201757.
@article{article, author = {Fumi\'{c}, Ksenija and Belu\v{z}i\'{c}, Robert and \'{C}uk, Mario and Pavkov, Tea and Kloor, Doris and Bari\'{c}, Ivo and Miji\'{c}, Ivana and Vugrek, Oliver}, year = {2007}, pages = {347-351}, DOI = {10.1038/sj.ejhg.5201757}, keywords = {AdoHcyase, recombinant protein, thermo sensitivity, circular dichroism, vascular disease}, journal = {European journal of human genetics}, doi = {10.1038/sj.ejhg.5201757}, volume = {15}, number = {3}, issn = {1018-4813}, title = {Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3}, keyword = {AdoHcyase, recombinant protein, thermo sensitivity, circular dichroism, vascular disease} }
@article{article, author = {Fumi\'{c}, Ksenija and Belu\v{z}i\'{c}, Robert and \'{C}uk, Mario and Pavkov, Tea and Kloor, Doris and Bari\'{c}, Ivo and Miji\'{c}, Ivana and Vugrek, Oliver}, year = {2007}, pages = {347-351}, DOI = {10.1038/sj.ejhg.5201757}, keywords = {AdoHcyase, recombinant protein, thermo sensitivity, circular dichroism, vascular disease}, journal = {European journal of human genetics}, doi = {10.1038/sj.ejhg.5201757}, volume = {15}, number = {3}, issn = {1018-4813}, title = {Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3}, keyword = {AdoHcyase, recombinant protein, thermo sensitivity, circular dichroism, vascular disease} }

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


Citati:





    Contrast
    Increase Font
    Decrease Font
    Dyslexic Font