Letno poročilo 2005
Letno poročilo 2005
Letno poročilo 2005
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sevov mikroorganizmov, predvsem ekstremofilnih<br />
gliv in jo redno dopolnjujemo z novimi<br />
izolati.<br />
BIBLIOGRAFIJA<br />
18 izvirnih znanstvenih ~lankov<br />
1 kratki znanstveni prispevek<br />
1 samostojni znanstveni sestavek v<br />
monografiji<br />
3 objavljeni znanstveni prispevki na<br />
konferencah<br />
23 objavljenih povzetkov znanstvenih<br />
prispevkov na konferencah<br />
1 patentna prijava<br />
1 patent<br />
5 predavanj na tujih univerzah<br />
1 prispevek na konferenci brez natisa<br />
8 diplom<br />
1 doktorat<br />
GLAVNI DOSE@KI V LETU <strong>2005</strong><br />
V letu <strong>2005</strong> smo v sodelovanju z drugimi<br />
laboratoriji na Kemijskem in{titutu in zunanjimi<br />
uporabniki pridobili preto~ni citometer s<br />
sorterjem in CD spektrometer, dve pomembni<br />
aparaturi za raziskave v molekularni in strukturni<br />
biologiji.<br />
V zvezi z raziskavami receptorjev LPS oz.<br />
inhibicijo signalizacije Toll-u podobnih receptorjev<br />
(TLR) smo v lanskem letu napravili<br />
pomemben korak naprej, saj smo s pomo~jo<br />
fluorescen~nih prob pokazali na pomen<br />
hidrofobnih interakcij pri prepoznavanju in na<br />
tej osnovi testirali vezavo vrste spojin, za katere<br />
je bilo prej `e ugotovljeno, da inhibirajo celi~no<br />
signalizacijo preko NF-kB. Vlogo hidrofobnih<br />
interakcij v vezavnem `epu smo potrdili tudi z<br />
usmerjenimi mutantami MD-2, ki je vezan na<br />
izvenceli~no domeno TLR4. Vezavo enakih spojin<br />
kot na MD-2 smo analizirali tudi na homologa<br />
Der p2 in GM2-AP in ugotovili, da je GM2-AP<br />
najbr` bolj primeren strukturni model za MD-<br />
2.<br />
Poleg inhibicije receptorja lahko nevtralizacijo<br />
delovanja endotoksina dose`emo tudi s<br />
spojinami, ki se direktno ve`ejo na LPS in<br />
Laboratorij za biotehnologijo<br />
Laboratory of Biotechnology<br />
lection, with more than 3,000 different strains,<br />
with emphasis on extremophiles, which is regularly<br />
expanded by new species isolated from<br />
their natural environment.<br />
BIBLIOGRAPHY<br />
18 Original Scientific Articles<br />
1 Review Article<br />
1 Independent Scientific Component Part<br />
in a Monograph<br />
3 Published Scientific Conference Contributions<br />
23 Published Scientific Conference Contribution<br />
Abstracts<br />
1 Patent Application<br />
1 Patent<br />
5 Invited Lectures at Foreign Universities<br />
1 Unpublished Conference Contribution<br />
8 Undergraduate Theses<br />
1 Doctoral Dissertation<br />
IMPORTANT ACHIEVEMENTS IN <strong>2005</strong><br />
In <strong>2005</strong> a flow cytometer with cell sorting ability<br />
and a CD spectrometer were purchased with<br />
the help of other Laboratories of the National<br />
Institute of Chemistry as well as other users.<br />
The new equipment is very important for research<br />
in molecular and structural biology.<br />
In the research field on LPS receptors or inhibition<br />
of signalization by Toll-like receptors (TLR)<br />
an important step forward was achieved. With<br />
the help of fluorescent probes we succeeded<br />
to prove the importance of hydrophobic interactions<br />
in recognition of LPS and on this basis<br />
we tested binding of a number of compounds,<br />
previously known to inhibit cell signalization via<br />
NF-kB. The role of hydrophobic interactions in<br />
the binding pocket was confirmed also with<br />
point mutations of MD2, which is associated<br />
to the extracellular domain of TLR4. The binding<br />
of the same compounds as on MD2 was<br />
also analyzed on the homologues Der p2 and<br />
GM2-AP and found that GM2-AP is probably a<br />
more suitable structural model for MD2.<br />
In addition to receptor inhibiton it is possible<br />
to neutralize the endotoxin activity also by com-<br />
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