Abstract
The cell wall of fungi is a highly complex structure consisting of a network of polysaccharides in which a plethora of different proteins are embedded. It is one of the major organelles of the cell surrounding it like an armor which protects from environmental stresses like osmotic pressure and defines the shape and physical strength of the fungal cell. It is crucial for colonization and infection since it defines the interface between host and pathogen. No similar structure is present in the host, therefore it defines a prime target for drug development. In this context, it has been shown that cell surface proteins are required for adhesion to host cells. The fact, that both pathogenic fungi, like Candida albicans as well as non-pathogenic fungi, like Saccharomyces cerevisiae, in general, have a very similar polysaccharide structure but differ significantly in their protein composition which underscores the importance of cell wall proteins for pathogenesis. However, cell wall proteomics of fungi is a highly challenging task due to the complex biochemistry of these proteins. The extensive post-translational modifications and covalent attachment to the polysaccharide backbone of a large proportion of cell wall proteins makes it a demanding task to isolate and identify them. In this article, we describe the recent approaches that have been developed to describe cell wall dynamics and to isolate and identify cell wall proteins in the pathogenic yeast C. albicans.
Keywords: Candida albicans, cell wall, cell wall proteins, proteomics, transcriptomics, GPI-proteins, adhesion, Efg1p
Current Drug Targets
Title: Getting in Touch with Candida albicans: The Cell Wall of a Fungal Pathogen
Volume: 7 Issue: 4
Author(s): Kai Sohn, Jochen Schwenk, Constantin Urban, Johannes Lechner, Michael Schweikert and Steffen Rupp
Affiliation:
Keywords: Candida albicans, cell wall, cell wall proteins, proteomics, transcriptomics, GPI-proteins, adhesion, Efg1p
Abstract: The cell wall of fungi is a highly complex structure consisting of a network of polysaccharides in which a plethora of different proteins are embedded. It is one of the major organelles of the cell surrounding it like an armor which protects from environmental stresses like osmotic pressure and defines the shape and physical strength of the fungal cell. It is crucial for colonization and infection since it defines the interface between host and pathogen. No similar structure is present in the host, therefore it defines a prime target for drug development. In this context, it has been shown that cell surface proteins are required for adhesion to host cells. The fact, that both pathogenic fungi, like Candida albicans as well as non-pathogenic fungi, like Saccharomyces cerevisiae, in general, have a very similar polysaccharide structure but differ significantly in their protein composition which underscores the importance of cell wall proteins for pathogenesis. However, cell wall proteomics of fungi is a highly challenging task due to the complex biochemistry of these proteins. The extensive post-translational modifications and covalent attachment to the polysaccharide backbone of a large proportion of cell wall proteins makes it a demanding task to isolate and identify them. In this article, we describe the recent approaches that have been developed to describe cell wall dynamics and to isolate and identify cell wall proteins in the pathogenic yeast C. albicans.
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Cite this article as:
Sohn Kai, Schwenk Jochen, Urban Constantin, Lechner Johannes, Schweikert Michael and Rupp Steffen, Getting in Touch with Candida albicans: The Cell Wall of a Fungal Pathogen, Current Drug Targets 2006; 7 (4) . https://dx.doi.org/10.2174/138945006776359395
DOI https://dx.doi.org/10.2174/138945006776359395 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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