Study on the interaction of artificial and natural food colorants with human serum albumin: A computational point of view. (June 2015)
- Record Type:
- Journal Article
- Title:
- Study on the interaction of artificial and natural food colorants with human serum albumin: A computational point of view. (June 2015)
- Main Title:
- Study on the interaction of artificial and natural food colorants with human serum albumin: A computational point of view
- Authors:
- Masone, Diego
Chanforan, Céline - Abstract:
- Abstract : Graphical abstract: Abstract : Highlights: High amounts of artificial food colorants present in infants' diets. Children behavioral problems related with ACs point to attention disorders. Comparison of HSA binding affinity to ACs and their natural industrial equivalents. H-bonding is stronger for the five ACs studied than their natural equivalents. Abstract: Due to the high amount of artificial food colorants present in infants' diets, their adverse effects have been of major concern among the literature. Artificial food colorants have been suggested to affect children's behavior, being hyperactivity the most common disorder. In this study we compare binding affinities of a group of artificial colorants (sunset yellow, quinoline yellow, carmoisine, allura red and tartrazine) and their natural industrial equivalents (carminic acid, curcumin, peonidin-3-glucoside, cyanidin-3-glucoside) to human serum albumin (HSA) by a docking approach and further refinement through atomistic molecular dynamics simulations. Due to the protein–ligand conformational interface complexity, we used collective variable driven molecular dynamics to refine docking predictions and to score them according to a hydrogen-bond criterion. With this protocol, we were able to rank ligand affinities to HSA and to compare between the studied natural and artificial food additives. Our results show that the five artificial colorants studied bind better to HSA than their equivalent natural options, inAbstract : Graphical abstract: Abstract : Highlights: High amounts of artificial food colorants present in infants' diets. Children behavioral problems related with ACs point to attention disorders. Comparison of HSA binding affinity to ACs and their natural industrial equivalents. H-bonding is stronger for the five ACs studied than their natural equivalents. Abstract: Due to the high amount of artificial food colorants present in infants' diets, their adverse effects have been of major concern among the literature. Artificial food colorants have been suggested to affect children's behavior, being hyperactivity the most common disorder. In this study we compare binding affinities of a group of artificial colorants (sunset yellow, quinoline yellow, carmoisine, allura red and tartrazine) and their natural industrial equivalents (carminic acid, curcumin, peonidin-3-glucoside, cyanidin-3-glucoside) to human serum albumin (HSA) by a docking approach and further refinement through atomistic molecular dynamics simulations. Due to the protein–ligand conformational interface complexity, we used collective variable driven molecular dynamics to refine docking predictions and to score them according to a hydrogen-bond criterion. With this protocol, we were able to rank ligand affinities to HSA and to compare between the studied natural and artificial food additives. Our results show that the five artificial colorants studied bind better to HSA than their equivalent natural options, in terms of their H-bonding network, supporting the hypothesis of their potential risk to human health. … (more)
- Is Part Of:
- Computational biology and chemistry. Volume 56(2015)
- Journal:
- Computational biology and chemistry
- Issue:
- Volume 56(2015)
- Issue Display:
- Volume 56, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 56
- Issue:
- 2015
- Issue Sort Value:
- 2015-0056-2015-0000
- Page Start:
- 152
- Page End:
- 158
- Publication Date:
- 2015-06
- Subjects:
- Food colorants -- Human serum albumin -- Docking -- Molecular dynamics
Chemistry -- Data processing -- Periodicals
Biology -- Data processing -- Periodicals
Biochemistry -- Data processing
Biology -- Data processing
Molecular biology -- Data processing
Periodicals
Electronic journals
542.85 - Journal URLs:
- http://www.sciencedirect.com/science/journal/14769271 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.compbiolchem.2015.04.006 ↗
- Languages:
- English
- ISSNs:
- 1476-9271
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3390.576700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8344.xml