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Zinc and copper binding proteins in human milk
The American Journal of Clinical Nutrition
|December 1, 1982
Summary
Researchers identified proteins binding zinc and copper in human milk, determining their distribution. Casein, serum albumin, low molecular weight forms, and fat are key binding components affecting infant bioavailability.
Area of Science:
- Biochemistry
- Human Nutrition
- Trace Element Metabolism
Background:
- Human milk is a vital source of essential trace elements like zinc and copper for infant development.
- Understanding the binding proteins and distribution of these minerals is crucial for assessing their bioavailability.
- Previous studies have indicated the presence of various binding fractions, but detailed characterization is ongoing.
Purpose of the Study:
- To fractionate and identify proteins that bind zinc and copper in human milk.
- To determine the distribution of zinc and copper among these identified binding compounds.
- To hypothesize on the factors influencing the distribution and potential bioavailability of these trace elements.
Main Methods:
- Ultracentrifugation was used to separate casein.
- Gel filtration and ion-exchange chromatography were employed to isolate other binding proteins.
- Gel electrophoresis was utilized for protein identification.
- Quantification of zinc and copper distribution across different fractions was performed.
Main Results:
- Casein bound 14% of total zinc and 28% of total copper.
- Serum albumin was identified as a binding protein, accounting for 28% of zinc and 39% of copper.
- A significant portion of zinc (29%) and copper (24%) was found in low molecular weight forms.
- Zinc (29%) and copper (9%) were also associated with the milk fat fraction.
Conclusions:
- Human milk contains multiple binding compounds for zinc and copper, including casein, serum albumin, low molecular weight fractions, and fat.
- The relative distribution of zinc and copper among these binding compounds is influenced by their concentrations and association constants.
- This distribution pattern may significantly impact the bioavailability of zinc and copper for the infant.