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Peptides Released from Foremilk and Hindmilk Proteins by Breast Milk Proteases Are Highly Similar

Human milk contains active proteases that initiate hydrolysis of milk proteins within the mammary gland. Milk expressed at the beginning of feeding is known as foremilk and that at the end of feeding is known as hindmilk. As hindmilk contains higher fat, vitamins A and E, and higher calories than fo...

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Autores principales: Nielsen, Søren D., Beverly, Robert L., Dallas, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673630/
https://www.ncbi.nlm.nih.gov/pubmed/29164128
http://dx.doi.org/10.3389/fnut.2017.00054
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author Nielsen, Søren D.
Beverly, Robert L.
Dallas, David C.
author_facet Nielsen, Søren D.
Beverly, Robert L.
Dallas, David C.
author_sort Nielsen, Søren D.
collection PubMed
description Human milk contains active proteases that initiate hydrolysis of milk proteins within the mammary gland. Milk expressed at the beginning of feeding is known as foremilk and that at the end of feeding is known as hindmilk. As hindmilk contains higher fat, vitamins A and E, and higher calories than foremilk, feeding only hindmilk initially and reserving foremilk for later are practiced in some neonatal intensive care units. This study investigated the difference in peptide profiles, predicted milk protease activities, and bioactive peptides between foremilk and hindmilk. Bioactive peptides are short fragments of proteins that influence biological processes. Four mothers pumped 10 mL of their foremilk and 10 mL of their hindmilk into iced containers prepared with antiproteases and the samples were immediately frozen. The peptide profile of each sample was analyzed by liquid chromatography nano-electrospray ionization Orbitrap Fusion tandem mass spectrometry. Peptide abundance (sum of ion intensities) and count (number of unique peptide sequences) in each milk sample were determined from this analysis. The specific enzymes that participated in peptide release were predicted based on the amino acids positioned at each cleavage site. Peptide bioactivity was predicted based on homology to a known functional peptide database and two bioactivity prediction algorithms. Hindmilk contained a higher count of peptides than foremilk. The higher number of unique peptide sequences in hindmilk was related to hydrolysis of β-casein, osteopontin, α(s1)-casein and mucin-1 via plasmin and elastase cleavage, and possible aminopeptidase and carboxypeptidase activities. Though hindmilk contained a greater number of peptides than foremilk, the overall peptide abundance did not differ and most of the total peptide abundance derived from peptide sequences that were present in both milk types. The presence of higher numbers of predicted bioactive peptides in the hindmilk could indicate that the practice of providing hindmilk rather than foremilk to premature infants could positively impact health outcomes; however, as there are few differences in overall peptide abundance, the overall effect is likely limited.
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spelling pubmed-56736302017-11-21 Peptides Released from Foremilk and Hindmilk Proteins by Breast Milk Proteases Are Highly Similar Nielsen, Søren D. Beverly, Robert L. Dallas, David C. Front Nutr Nutrition Human milk contains active proteases that initiate hydrolysis of milk proteins within the mammary gland. Milk expressed at the beginning of feeding is known as foremilk and that at the end of feeding is known as hindmilk. As hindmilk contains higher fat, vitamins A and E, and higher calories than foremilk, feeding only hindmilk initially and reserving foremilk for later are practiced in some neonatal intensive care units. This study investigated the difference in peptide profiles, predicted milk protease activities, and bioactive peptides between foremilk and hindmilk. Bioactive peptides are short fragments of proteins that influence biological processes. Four mothers pumped 10 mL of their foremilk and 10 mL of their hindmilk into iced containers prepared with antiproteases and the samples were immediately frozen. The peptide profile of each sample was analyzed by liquid chromatography nano-electrospray ionization Orbitrap Fusion tandem mass spectrometry. Peptide abundance (sum of ion intensities) and count (number of unique peptide sequences) in each milk sample were determined from this analysis. The specific enzymes that participated in peptide release were predicted based on the amino acids positioned at each cleavage site. Peptide bioactivity was predicted based on homology to a known functional peptide database and two bioactivity prediction algorithms. Hindmilk contained a higher count of peptides than foremilk. The higher number of unique peptide sequences in hindmilk was related to hydrolysis of β-casein, osteopontin, α(s1)-casein and mucin-1 via plasmin and elastase cleavage, and possible aminopeptidase and carboxypeptidase activities. Though hindmilk contained a greater number of peptides than foremilk, the overall peptide abundance did not differ and most of the total peptide abundance derived from peptide sequences that were present in both milk types. The presence of higher numbers of predicted bioactive peptides in the hindmilk could indicate that the practice of providing hindmilk rather than foremilk to premature infants could positively impact health outcomes; however, as there are few differences in overall peptide abundance, the overall effect is likely limited. Frontiers Media S.A. 2017-11-02 /pmc/articles/PMC5673630/ /pubmed/29164128 http://dx.doi.org/10.3389/fnut.2017.00054 Text en Copyright © 2017 Nielsen, Beverly and Dallas. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Nielsen, Søren D.
Beverly, Robert L.
Dallas, David C.
Peptides Released from Foremilk and Hindmilk Proteins by Breast Milk Proteases Are Highly Similar
title Peptides Released from Foremilk and Hindmilk Proteins by Breast Milk Proteases Are Highly Similar
title_full Peptides Released from Foremilk and Hindmilk Proteins by Breast Milk Proteases Are Highly Similar
title_fullStr Peptides Released from Foremilk and Hindmilk Proteins by Breast Milk Proteases Are Highly Similar
title_full_unstemmed Peptides Released from Foremilk and Hindmilk Proteins by Breast Milk Proteases Are Highly Similar
title_short Peptides Released from Foremilk and Hindmilk Proteins by Breast Milk Proteases Are Highly Similar
title_sort peptides released from foremilk and hindmilk proteins by breast milk proteases are highly similar
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673630/
https://www.ncbi.nlm.nih.gov/pubmed/29164128
http://dx.doi.org/10.3389/fnut.2017.00054
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