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PMID: 8022864 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Critical steps in fungal cell wall synthesis: strategies for their inhibition.

Pharmacology & therapeutics ·Vol. 60 ·No. 2 ·1993-11-00 ·Pages 337-45

Gozalbo D, Elorza MV, Sanjuan R, Marcilla A, Valentín E, Sentandreu R

Abstract

Development of new effective antifungal drugs is limited by the absence of specific target sites in the fungal cells. Knowledge of the fungal cell wall structure and biosynthesis is of interest in searching for a potential target site for new chemotherapeutic agents. Our group has demonstrated that the fungal cell wall is a metabolically active structure where interaction between distinct components occurs to give rise to the mature cell wall structure. Mannoproteins play an essential role in the cell wall organization, and there is evidence for the formation of covalent bonds between these molecules and the structural polymers (glucans and chitin) outside the plasma membrane. Such interactions, which specifically occur at the fungal cell wall, are of great interest in defining target sites for potential new chemotherapeutic agents, which may inhibit the interactions and, thus, lead to a defective cell wall formation and cell death.

MeSH Terms
Antifungal Agents/pharmacology Candida albicans/drug effects,metabolism,ultrastructure Cell Wall/chemistry,drug effects,metabolism Fungi/drug effects,metabolism,ultrastructure Humans Membrane Glycoproteins/biosynthesis,chemistry,physiology Molecular Structure Polysaccharides/analysis,biosynthesis
Chemicals
Antifungal Agents Membrane Glycoproteins Polysaccharides mannoproteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Gozalbo D
Secció de Microbiologia, Facultat de Farmàcia, Universitat de València, Spain.
Elorza M V
Sanjuan R
Marcilla A
Valentín E
Sentandreu R
Article Info
Journal
Pharmacology & therapeutics
Abbr.
Pharmacol Ther
ISSN
0163-7258
Published
1993-11-00
Pages
337-45
Language
English
Region
England
NLM ID
7905840
Subset
IM
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