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Y-27632 Enriches the Yield of Human Melanocytes from Adult Skin Tissues
Published on: July 8, 2020
Fungal melanins differ in planar stacking distances.
Arturo Casadevall1, Antonio Nakouzi, Pier R Crippa
1Department of Microbiology and Immunology, Division of Infectious Diseases, Albert Einstein College of Medicine, Bronx, New York, United States of America. arturo.casadevall@einstein.yu.edu
Plos One
|February 24, 2012
Summary
Structural analysis of fungal melanins using X-ray diffraction reveals distinct stacking distances. These findings suggest a universal diffracting unit in melanins, aiding in the characterization of this complex pigment.
Area of Science:
- Biophysics
- Materials Science
- Mycology
Background:
- Melanins are challenging to study due to their amorphous and insoluble nature.
- Limited structural techniques exist for analyzing melanin.
- Current models propose stacked planar structures, often analyzed by X-ray diffraction.
Purpose of the Study:
- To structurally characterize fungal melanins using X-ray diffraction.
- To compare the inferred stacking parameters of different fungal melanins.
- To investigate the universal structural features of melanins.
Main Methods:
- X-ray diffraction analysis of melanins isolated from Cryptococcus neoformans, Aspergillus niger, Wangiella dermatitides, and Coprinus comatus.
- Comparison of diffraction parameters with synthetic melanin and neuromelanin.
- Exclusion of capsular polysaccharide interference in Cryptococcus neoformans analysis.
Main Results:
- Fungal melanins exhibit inferred stacking distances intermediate between synthetic melanin and neuromelanin.
- A broad non-Bragg feature was observed in the capsular polysaccharide of C. neoformans, suggesting gel organization.
- The stacking peak appears to be a universal feature distinguishing melanins.
Conclusions:
- Fungal melanins possess unique stacking distances compared to other melanin types.
- All melanins likely share a fundamental diffracting unit of planar graphitic assemblies.
- The stacking peak is a potential characteristic feature for melanin identification and characterization.
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