Extensive in vivo human milk peptidomics reveals specific proteolysis yielding protective antimicrobial peptides

David C. Dallas, Andres Guerrero, Nora Khaldi, Patricia A. Castillo, William F. Martin, Jennifer T. Smilowitz, Charles L Bevins, Daniela Barile, J. Bruce German, Carlito B Lebrilla

Research output: Contribution to journalArticle

71 Citations (Scopus)

Abstract

Milk is traditionally considered an ideal source of the basic elemental nutrients required by infants. More detailed examination is revealing that milk represents a more functional ensemble of components with benefits to both infants and mothers. A comprehensive peptidomics method was developed and used to analyze human milk yielding an extensive array of protein products present in the fluid. Over 300 milk peptides were identified originating from major and many minor protein components of milk. As expected, the majority of peptides derived from β-casein, however no peptide fragments from the major milk proteins lactoferrin, α-lactalbumin, and secretory immunoglobulin A were identified. Proteolysis in the mammary gland is selective - released peptides were drawn only from specific proteins and typically from only select parts of the parent sequence. A large number of the peptides showed significant sequence overlap with peptides with known antimicrobial or immunomodulatory functions. Antibacterial assays showed the milk peptide mixtures inhibited the growth of Escherichia coli and Staphylococcus aureus. The predigestion of milk proteins and the consequent release of antibacterial peptides may provide a selective advantage through evolution by protecting both the mother's mammary gland and her nursing offspring from infection.

Original languageEnglish (US)
Pages (from-to)2295-2304
Number of pages10
JournalJournal of Proteome Research
Volume12
Issue number5
DOIs
StatePublished - May 3 2013

Fingerprint

Proteolysis
Human Milk
Peptides
Milk Proteins
Milk
Human Mammary Glands
Mothers
Lactalbumin
Secretory Immunoglobulin A
Protein Array Analysis
Peptide Fragments
Proteins
Lactoferrin
Nursing
Caseins
Escherichia coli
Nutrients
Staphylococcus aureus
Assays
Food

Keywords

  • functional peptide
  • human milk
  • peptidomics
  • plasmin
  • protease

ASJC Scopus subject areas

  • Biochemistry
  • Chemistry(all)

Cite this

Dallas, D. C., Guerrero, A., Khaldi, N., Castillo, P. A., Martin, W. F., Smilowitz, J. T., ... Lebrilla, C. B. (2013). Extensive in vivo human milk peptidomics reveals specific proteolysis yielding protective antimicrobial peptides. Journal of Proteome Research, 12(5), 2295-2304. https://doi.org/10.1021/pr400212z

Extensive in vivo human milk peptidomics reveals specific proteolysis yielding protective antimicrobial peptides. / Dallas, David C.; Guerrero, Andres; Khaldi, Nora; Castillo, Patricia A.; Martin, William F.; Smilowitz, Jennifer T.; Bevins, Charles L; Barile, Daniela; German, J. Bruce; Lebrilla, Carlito B.

In: Journal of Proteome Research, Vol. 12, No. 5, 03.05.2013, p. 2295-2304.

Research output: Contribution to journalArticle

Dallas, DC, Guerrero, A, Khaldi, N, Castillo, PA, Martin, WF, Smilowitz, JT, Bevins, CL, Barile, D, German, JB & Lebrilla, CB 2013, 'Extensive in vivo human milk peptidomics reveals specific proteolysis yielding protective antimicrobial peptides', Journal of Proteome Research, vol. 12, no. 5, pp. 2295-2304. https://doi.org/10.1021/pr400212z
Dallas, David C. ; Guerrero, Andres ; Khaldi, Nora ; Castillo, Patricia A. ; Martin, William F. ; Smilowitz, Jennifer T. ; Bevins, Charles L ; Barile, Daniela ; German, J. Bruce ; Lebrilla, Carlito B. / Extensive in vivo human milk peptidomics reveals specific proteolysis yielding protective antimicrobial peptides. In: Journal of Proteome Research. 2013 ; Vol. 12, No. 5. pp. 2295-2304.
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