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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 />

143

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