Naslov
Juvenile Rheumatoid Arthritis is Associated with Decreased Activity of Lectins in Serum

Autori
Lauc, Gordan ; Dumić, Jerka ; Flögel, Mirna

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
Book of Abstracts / Flögel, M. i sur - Zagreb : Hrvatsko biokemijsko društvo, 2000, 105-105

Skup
HB2000, Silver Jubilee Meeting of the Croatian Biochemical Society

Mjesto i datum
Zagreb, Hrvatska, 13.10.2000. - 15.10.2000

Vrsta sudjelovanja
Poster

Vrsta recenzije
Domaća recenzija

Ključne riječi
Glycoproteins; Juvenile rheumatoid arthritis; Lectins

Sažetak
Over a half of all known proteins contain covalently linked oligosaccharide structures that presumably perform some specific physiological functions. Due to the lack of adequate methods, until recently only little was known about the role of oligosaccharide structures of glycoconjugates. However, in the recent years it was convincingly demonstrated that at least some of these structures are of utmost importance. One of the principal ways how oligosaccharides perform their functions is through interactions with their specific receptors named lectins. Recently we have developed glycoprobes, a novel set of compounds that enable direct measurement of lectin activity in complex biological samples. The glycoprobe consists of three vital parts: (i) glycan; (ii) digoxin tag; and (iii) photoreactive crosslinker. When incubated in dark, oligosaccharide part of the glycoprobe forms a complex with lectin. After illumination, covalent link between the probe and the lectin is formed resulting in a digoxin-tagged lectin. Using antibodies against digoxin, this complex can easily be identified by Western blots. Glycoprobes containing Man9 oligosaccharide and YEE(ahGalNAc)3 glycopeptide were prepared and used to analyze lectin activity in sera of 20 patients with juvenile rheumatoid arthritis and 20 control sera. Human serum (75 μg of total protein) was incubated in the presence of 0.8 mM mannose- or GalNAc-glycoprobe in dark for 60 min. After crosslinking by UV-illumination, proteins were separated by 8% SDS PAGE, transferred onto PVDF membranes and analyzed with anti-digoxin antibodies. As expected, we were able to detect several lectins that specifically bound glycoprobes. The variability of lectin content and activity was surprisingly high in both patients with juvenile rheumatoid arthritis and controls. Some of the changes were apparently the consequence of natural variability, but for several specific lectins we were able to demonstrate significantly different activities between the control group and patients suffering from juvenile rheumatoid arthritis.

Izvorni jezik
Engleski

Znanstvena područja
Biologija

POVEZANOST RADA