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Multiplexed activity-based protein profiling of the human pathogen Aspergillus fumigatus reveals large functional changes upon exposure to human serum
- Source :
- The Journal of biological chemistry. 287(40)
- Publication Year :
- 2012
-
Abstract
- Environmental adaptability is critical for survival of the fungal human pathogen Aspergillus fumigatus in the immunocompromised host lung. We hypothesized that exposure of the fungal pathogen to human serum would lead to significant alterations to the organism's physiology, including metabolic activity and stress response. Shifts in functional pathway and corresponding enzyme reactivity of A. fumigatus upon exposure to the human host may represent much needed prognostic indicators of fungal infection. To address this, we employed a multiplexed activity-based protein profiling (ABPP) approach coupled to quantitative mass spectrometry-based proteomics to measure broad enzyme reactivity of the fungus cultured with and without human serum. ABPP showed a shift from aerobic respiration to ethanol fermentation and utilization over time in the presence of human serum, which was not observed in serum-free culture. Our approach provides direct insight into this pathogen's ability to survive, adapt, and proliferate. Additionally, our multiplexed ABPP approach captured a broad swath of enzyme reactivity and functional pathways and provides a method for rapid assessment of the A. fumigatus response to external stimuli.
- Subjects :
- Lung Diseases
Proteomics
Serum
Time Factors
Genomics and Proteomics
Cellular respiration
Protein Array Analysis
Human pathogen
Biochemistry
Models, Biological
Culture Media, Serum-Free
Mass Spectrometry
Aspergillus fumigatus
Microbiology
Fungal Proteins
Gene Expression Regulation, Fungal
parasitic diseases
Aspergillosis
Humans
skin and connective tissue diseases
Molecular Biology
Pathogen
Lung
Fungal protein
Aspergillus
biology
Activity-based proteomics
Cell Biology
biology.organism_classification
bacterial infections and mycoses
Models, Chemical
Subjects
Details
- ISSN :
- 1083351X
- Volume :
- 287
- Issue :
- 40
- Database :
- OpenAIRE
- Journal :
- The Journal of biological chemistry
- Accession number :
- edsair.doi.dedup.....24882f1ac93cac0aa4cb700767d18a9a