Abstract
ABSTRACT The ATP-binding cassette (ABC) genes
encode the largest family of transmembrane proteins.
ABC transporters translocate a wide variety of substrates
across membranes, but their physiological function
is often incompletely understood. We describe a
new method to study the substrate spectrum of ABC
transporters: We incubate extracts of mouse urine with
membrane vesicles prepared from Spodoptera frugiperda
Sf9 insect cells overproducing an ABC transporter
and determine the compounds transported into
the vesicles by LC/MS-based metabolomics. We illustrate
the power of this simple “transportomics” approach
using ABCC2, a protein present at sites of
uptake and elimination. We identified many new substrates
of ABCC2 in urine. These included glucuronides
of plant-derived xenobiotics, a class of compounds
to which humans are exposed on a daily basis.
Moreover, we show that the excretion of these compounds
in vivo depends on ABCC2: compared to wildtype
mice, the urinary excretion of several glucuronides
was increased up to 20-fold in Abcc2 / mice. Transportomics
has broad applicability, as it is not restricted
to urine and can be applied to other ATP-dependent
transport proteins as well.
Original language | English |
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Pages (from-to) | 738-747 |
Number of pages | 10 |
Journal | FASEB Journal |
Volume | 26 |
DOIs | |
Publication status | Published - 2013 |