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An approach to characterize the membrane proteome of Candida albicans

: Rupp, S.


Future microbiology 5 (2010), No.2, pp.147-151
ISSN: 1746-0913
ISSN: 1746-0921
Journal Article
Fraunhofer IGB ()
candida albicans

Evaluation of: Cabezon V, Llama-Palacios A, Nombela C, Monteoliva L, Gil C: Analysis of Candida albicans plasma membrane proteome. Proteomics 9, 4770-4786 (2009). The opportunistic human fungal pathogen Candida albicans causes a wide variety of infections, including deep systemic infection. The C. albicans plasma membrane is an important interface in the host-pathogen relationship. Plasma membrane proteins mediate a variety of functions, including sensing and signaling to the external environment, in which the glycosylphosphatidylinositol (GPI)-anchored membrane proteins play a crucial role. A subproteomic approach to obtain a global picture of the protein composition of the C. albicans plasma membrane was developed, and different strategies were tested in order to extract the largest number of yeast plasma membrane proteins and GPI-anchored membrane proteins. These methods involved protoplast generation, mechanical disruption, ultracentrifugation in sucrose gradients and Na2CO3 treatments. To isolate GPI-anchored proteins two additional steps were performed: two-phase separation and phosphatidylinositol-phospholipase C treatment. After liquid chromatography tandem mass spectrometry analysis using both a MALDI-TOF/TOF and a linear ion trap quadrupole, a total of 214 membrane proteins were identified, including 41 already described as plasma membrane proteins, 20 plasma membrane-associated proteins and 22 proteins with unknown membrane localization. Bioinformatic analysis revealed that this set of C. albicans membrane proteins is highly enriched in proteins involved in biopolymer biosynthesis or transport processes. Furthermore, following phosphatidylinositol-phospholipase C treatment, 12 GPI-anchored membrane proteins were released and identified; most of them are associated with cell wall glucan synthesis and maintenance or are virulence factors, such as phospholipases or aspartyl proteinases.