Veränderungen des Lipidstoffwechsels bei HIV-Patienten unter der Therapie mit Proteaseinhibitoren View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2000

AUTHORS

G. Behrens , H. H.-J. Schmidt , J. Genschel , M. Stoll , A. Dejam , R. Haas , M. P. Manns , R. E. Schmidt

ABSTRACT

Die HIV-1 Protease besteht aus zwei 99 Aminosäuren Untereinheiten, die ein Homodimer bilden und Aspartylprotease-Aktivität besitzen. HIV-1 Proteaseinhibitoren binden mit hoher Affinität an die katalytische Domäne der HIV-1 Protease und verhindern so die Spaltung von HIV-Proteinen in infizierten Zellen. Durch die Reifungshemmung des Virus fällt die Virusmenge von HIV im Blut und in den Lymphknoten unter der Behandlung mit Proteaseinhibitoren rasch ab. Die vier zur Zeit zugelassenen Proteaseinhibitoren (Saquinavir, Indinavir, Ritonavir, Nelfìnavir) sind strukturell verwandte Substanzen, die die Spaltung von Vorläuferproteinen kompetetiv hemmen [9]. More... »

PAGES

344-349

Book

TITLE

HIV-Infekt

ISBN

978-3-642-64082-7
978-3-642-59683-4

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-3-642-59683-4_62

DOI

http://dx.doi.org/10.1007/978-3-642-59683-4_62

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1024437568


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