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. Author manuscript; available in PMC: 2011 Dec 28.
Published in final edited form as: Biochemistry. 2010 Dec 2;49(51):10854–10861. doi: 10.1021/bi101350x

Figure 4.

Figure 4

Effect of TM5 replacement on dimerization. (A) Schematic diagram of ABCC1F-HA and the ABCC1281N constructs with TM5 replaced with TM3 or TM9. The TMs are shown as boxes, and the amino acid sequences of TM3, TM5, and TM9 are shown in single-letter code. The MRPr1 epitope and the HA tag are shown as horizontal and vertical ovals, respectively. (B) Expression (top) and co-immunoprecipitation (middle and bottom) of the wild type and the mutant ABCC1281N constructs. The wild type and the mutant ABCC1281N constructs were transiently transfected into HEK293 cells with stable expression of ABCC1F-HA followed by co-immunoprecipitation with the HA antibody and Western blot analyses probed with antibody MRPr1. (C) Correlation of hydrophobicity with the level of co-immunoprecipitation. The hydrophobicity of TM3, TM5, and TM9 was calculated using an online program (http://www.expasy.ch/tools/protparam.html), and the GRAVY scores are shown. The co-immunoprecipitation levels of the wild type and the mutant ABCC1281N constructs in panel B were quantified using ScnImage and normalized to that of wild-type ABCC1281N.