TY - JOUR
T1 - Quantitative Targeted Absolute Proteomics for 28 Transporters in Brush-Border and Basolateral Membrane Fractions of Rat Kidney
AU - Uchida, Yasuo
AU - Toyohara, Takafumi
AU - Ohtsuki, Sumio
AU - Moriyama, Yoshinori
AU - Abe, Takaaki
AU - Terasaki, Tetsuya
N1 - Funding Information:
The authors would like to thank N. Funayama and A. Niitomi for their secretarial assistance. This study was supported in part by three Grants-in-Aid from the Japanese Society for the Promotion of Science (JSPS) for Scientific Research (S) (KAKENHI: 18109002), Scientific Research (A) (KAKENHI: 24249011), and Global COE Program. Regarding conflicts of interest, Tetsuya Terasaki and Sumio Ohtsuki are full professors at Tohoku University and Kumamoto University, respectively, and are also directors of Proteomedix Frontiers Company, Ltd. This study was not supported by Proteomedix Frontiers Company, Ltd., and their positions at Proteomedix Frontiers Company, Ltd. did not influence the design of the study, the collection of the data, the analysis or interpretation of the data, the decision to submit the manuscript for publication, or the writing of the manuscript, and did not present any financial conflicts. The other authors declare no competing interests.
Publisher Copyright:
© 2016 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - The purpose of the present study was to determine the absolute protein expression levels of various transporters in renal brush-border membrane (BBM) and basolateral membrane (BLM) fractions, in order to understand the quantitative differences in average transport activities among different transporters at each cellular membrane. BBM and BLM fractions of rat kidney were prepared and digested with trypsin, and simultaneous absolute quantification of 28 transporters and a BLM marker, Na+/K+-ATPase, was performed using our established quantitative-targeted absolute proteomics (QTAP) technique. In BBM fraction, the protein expression levels of bcrp, urat1, mate1, octl1, mrp4, mdr1a, and abca3 were 40.3, 22.2, 8.90, 4.85, 4.69, 3.22, and 0.976 fmol/μg protein, respectively. In BLM fraction, the protein expression levels of oat1, oat3, oct1, mrp6, and mrp1 were 10.6, 10.2, 4.59, 0.724, and 0.271 fmol/μg protein, respectively. The expression levels of abca2, abca4, abca5, abca12, abcb4, mrp5, abcc9, abcg1, abcg5, lat1, ntcp, pgt, oatp2b1, oatp1b2, oatp3a1, and oct3 were under the limit of quantification in both fractions. The quantitative transporter protein expression profiles at these membranes, as determined by QTAP analysis, should be helpful to understand the contributions of individual transporters to renal excretion of xenobiotics and endogenous compounds.
AB - The purpose of the present study was to determine the absolute protein expression levels of various transporters in renal brush-border membrane (BBM) and basolateral membrane (BLM) fractions, in order to understand the quantitative differences in average transport activities among different transporters at each cellular membrane. BBM and BLM fractions of rat kidney were prepared and digested with trypsin, and simultaneous absolute quantification of 28 transporters and a BLM marker, Na+/K+-ATPase, was performed using our established quantitative-targeted absolute proteomics (QTAP) technique. In BBM fraction, the protein expression levels of bcrp, urat1, mate1, octl1, mrp4, mdr1a, and abca3 were 40.3, 22.2, 8.90, 4.85, 4.69, 3.22, and 0.976 fmol/μg protein, respectively. In BLM fraction, the protein expression levels of oat1, oat3, oct1, mrp6, and mrp1 were 10.6, 10.2, 4.59, 0.724, and 0.271 fmol/μg protein, respectively. The expression levels of abca2, abca4, abca5, abca12, abcb4, mrp5, abcc9, abcg1, abcg5, lat1, ntcp, pgt, oatp2b1, oatp1b2, oatp3a1, and oct3 were under the limit of quantification in both fractions. The quantitative transporter protein expression profiles at these membranes, as determined by QTAP analysis, should be helpful to understand the contributions of individual transporters to renal excretion of xenobiotics and endogenous compounds.
KW - ABC transporters
KW - HPLC (high-performance/pressure liquid chromatography)
KW - drug transport
KW - mass spectrometry
KW - membrane transport
KW - membrane transporter
KW - proteins
KW - proteomics
KW - renal excretion
KW - solute transporters
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U2 - 10.1002/jps.24645
DO - 10.1002/jps.24645
M3 - Article
AN - SCOPUS:84941695186
SN - 0022-3549
VL - 105
SP - 1011
EP - 1016
JO - Journal of Pharmaceutical Sciences
JF - Journal of Pharmaceutical Sciences
IS - 2
ER -