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      Quantification of lactoferrin in breast milk by ultra-high performance liquid chromatography-tandem mass spectrometry with isotopic dilution

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          Abstract

          We developed a LC-MS/MS method for quantification of human lactoferrin in breast milk based on tryptic peptides and a synthetic isotopic peptide standard.

          Abstract

          We developed a LC-MS/MS method for quantification of human lactoferrin in breast milk based on tryptic peptides and a synthetic isotopic peptide standard. The signature peptides were obtained from tryptic breast milk. They were screened by computational prediction using Biolynx software, and confirmed by database searching after analysis using liquid chromatography-quadrupole-time-of-flight tandem mass spectrometry (LC-Q-TOF-MS). The winged isotopic-labeled signature peptide was used as an internal standard to compensate the matrix effect. The spiking recovery of human lactoferrin ranged from 92.1% to 97.5%, and the relative standard deviation (RSD) was 3.4–4.7%. The limit of detection (LOD) and limit of quantitation (LOQ) were 1 mg/100 g and 3 mg/100 g in tryptic breast milk, respectively. The present testing method was sensitive and selective, and was successfully applied to human breast milk at different lactation stages in Beijing, China. The data revealed that levels of secreted lactoferrin decreased with the extension of lactation.

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          Human milk composition: nutrients and bioactive factors.

          This article provides an overview of the composition of human milk, its variation, and its clinical relevance. The composition of human milk is the biological norm for infant nutrition. Human milk also contains many hundreds to thousands of distinct bioactive molecules that protect against infection and inflammation and contribute to immune maturation, organ development, and healthy microbial colonization. Some of these molecules (eg, lactoferrin) are being investigated as novel therapeutic agents. Human milk changes in composition from colostrum to late lactation, within feeds, by gestational age, diurnally, and between mothers. Feeding infants with expressed human milk is increasing. Copyright © 2013 Elsevier Inc. All rights reserved.
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            Is Open Access

            Selected reaction monitoring for quantitative proteomics: a tutorial

            Systems biology relies on data sets in which the same group of proteins is consistently identified and precisely quantified across multiple samples, a requirement that is only partially achieved by current proteomics approaches. Selected reaction monitoring (SRM)—also called multiple reaction monitoring—is emerging as a technology that ideally complements the discovery capabilities of shotgun strategies by its unique potential for reliable quantification of analytes of low abundance in complex mixtures. In an SRM experiment, a predefined precursor ion and one of its fragments are selected by the two mass filters of a triple quadrupole instrument and monitored over time for precise quantification. A series of transitions (precursor/fragment ion pairs) in combination with the retention time of the targeted peptide can constitute a definitive assay. Typically, a large number of peptides are quantified during a single LC-MS experiment. This tutorial explains the application of SRM for quantitative proteomics, including the selection of proteotypic peptides and the optimization and validation of transitions. Furthermore, normalization and various factors affecting sensitivity and accuracy are discussed.
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              Selected reaction monitoring-based proteomics: workflows, potential, pitfalls and future directions.

              Selected reaction monitoring (SRM) is a targeted mass spectrometry technique that is emerging in the field of proteomics as a complement to untargeted shotgun methods. SRM is particularly useful when predetermined sets of proteins, such as those constituting cellular networks or sets of candidate biomarkers, need to be measured across multiple samples in a consistent, reproducible and quantitatively precise manner. Here we describe how SRM is applied in proteomics, review recent advances, present selected applications and provide a perspective on the future of this powerful technology.
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                Author and article information

                Journal
                RSCACL
                RSC Advances
                RSC Adv.
                Royal Society of Chemistry (RSC)
                2046-2069
                2016
                2016
                : 6
                : 15
                : 12280-12285
                Affiliations
                [1 ]College of Chemical Engineering
                [2 ]Zhejiang University of Technology
                [3 ]Hangzhou
                [4 ]China
                [5 ]Zhejiang Provincial Center for Disease Control and Prevention
                Article
                10.1039/C5RA27243B
                51d25aaf-057a-4dec-af01-3f87ac5c4112
                © 2016
                History

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