Proteomic profiling of xenobiotic and nutrient transporters in human placenta of different gestational ages
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ABSTRACT: The placenta serves a critical role in nutrient uptake and waste elimination for the developing fetus and is responsible for the uptake and/or exchange of xenobiotics, including medications, between the maternal and fetal bloodstreams. Very little is understood about fetal drug and nutrient exposure during pregnancy and how it may change over the course of fetal development. The primary goal of this work was to profile the abundance of placental xenobiotic and nutrient transporters over the course of gestation using a data-independent analysis (DIA) proteomics approach. Building a deeper understanding of these proteins at the interface between the fetal and maternal bloodstreams will inform future studies designed to address questions regarding the safety and efficacy of therapeutics and nutrient supplements used during pregnancy. A total of 139 solute carrier (SLC) and ATP-cassette binding (ABC) transport proteins were identified across all samples, 80 of which were found in every sample (n = 34). Seventeen transport proteins (14 SLC, 3 ABC) were found to be significantly altered between trimesters during development. To the best of our knowledge, this study represents the first global proteomic characterization of placental membrane-associated proteins using DIA-MS proteomics and lays the groundwork for further advancements in the understanding of the membrane-associated proteome during fetal development.
ORGANISM(S): Homo Sapiens
SUBMITTER:
Eric Weaver
PROVIDER: PXD080148 | panorama | Thu Jun 25 00:00:00 BST 2026
REPOSITORIES: PanoramaPublic
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