Pregled bibliografske jedinice broj: 990291
Characterization of antithrombin III from human plasma by two-dimensional gel electrophoresis and capillary electrophoretic methods
Characterization of antithrombin III from human plasma by two-dimensional gel electrophoresis and capillary electrophoretic methods // ELECTROPHORESIS, 24 (2003), 24; 4282-4290 doi:10.1002/elps.200305651 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 990291 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Characterization of antithrombin III from human plasma by two-dimensional gel electrophoresis and capillary electrophoretic methods
Autori
Kremser, Leopold ; Brückner, Andrea ; Heger, Andrea ; Grunert, Tom ; Buchacher, Andrea ; Josic, Djuro ; Allmaier, Günter ; Rizzi, Andreas
Izvornik
ELECTROPHORESIS (0173-0835) 24
(2003), 24;
4282-4290
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Antithrombin III ; Capillary isoelectric focusing ; Capillary zone electrophoresis ; Glycoprotein microheterogeneity ; Two‐dimensional gel electrophoresis
Sažetak
The isoforms distribution of the glycoprotein antithrombin III (ATIII) derived from human plasma was investigated by means of isoelectric focusing (IEF) in polyacrylamide gels with immobilized pH gradients (IPG) and two‐dimensional gel electrophoresis (2‐DE) as well as capillary electrophoretic methods. It turned out that the presence of high concentrations of chaotropics (urea, thiourea) and zwitterionic detergents (3‐[(3‐cholamidepropyl)dimethylammonio]‐1‐propanesulfonate (CHAPS)) was decisive for attaining good resolution of the protein isoforms. Resolution by IPG‐IEF was obtained with excellent reproducibility and pI differences down to 0.01 pH units could be distinguished. ATIII‐α and ATIII‐β‐fractions preseparated by heparin affinity chromatography showed an analogous but shifted spot pattern consisting each of one major and three minor isoforms. The main isoforms of ATIII‐α and ATIII‐β exhibit pI values of 5.18 and 5.32, respectively, both values determined in the presence of high concentrations of urea. The pI difference of 0.14 pH units correspond to the effect of two sialic acids absent in ATIII‐β. The formation and occurrence of ATIII dimers and trimers turned out to be dependent on the sample preparation. The results obtained by 2‐DE were compared with those of capillary zone electrophoresis (CZE) and capillary IEF (CIEF). Quantitative analysis regarding the CZE separated isoforms of plasma derived ATIII yielded a content of about 70% ATIII‐α main isoform and about 6.6% of ATIII‐β. The pI values of ATIII determined by CIEF with internal calibration were in fair agreement with the pI values of the main isoforms achieved with 2‐DE.
Izvorni jezik
Engleski
Znanstvena područja
Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Ustanove:
Sveučilište u Rijeci - Odjel za biotehnologiju
Profili:
Đuro Josić
(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