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. 2021 Jun 2;11(12):3869–3878. doi: 10.1016/j.apsb.2021.05.030

Table 1.

Surrogate peptides used to quantify protein expression and MRM transitions used for LC–MS/MS detection in this study.

Protein Peptide sequence IS RT (min) Q1 [M+2H]2+ (Da) Q3 [M+H]+ (Da)
ATP7A LGAIDVER MRP2-H 12.8 436.7 759.4
ATP7B AIATQVGINK MRP2-H 11.4 507.8 759.4
CTR1 SQVSIR MRP2-H 7.9 345.2 474.3
MRP2 GINLSGGQK MRP2-H 10.0 437.2 703.4
MRP4 APVLFFDR MRP4-H 20.2 482.8 697.4
MATE1 HVGVILQR MRP4-H 11.4 461.3 685.4
OCT1 VPPADLK MRP2-H 9.0 370.2 640.4
OCT2 FLQGLVSK OCT2-H 16.1 446.3 503.3
OCT3 TTVATLGR MRP2-H 10.3 409.7 616.4
P-gp IATEAIENFR OCT2-H 15.8 582.3 979.5
MRP2-H GINL∗SGGQK 10.0 440.7 710.4
MRP4-H APVL∗FFDR 20.2 486.3 704.4
OCT2-H FLQGL∗VSK 16.1 449.8 751.5

Membrane protein fractions were digested with trypsin per Materials and Methods to quantify transporter expression. Multiple reaction monitoring transitions used for detection are listed as doubly-charged parent ion (Q1) and singly charged fragment ion (Q3) used for quantification. ∗13C/16N heavy isotope labeled amino acid internal standards (IS). RT, retention time for liquid chromatography method. –Not applicable.