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. 2017 Mar 10;292(20):8279–8290. doi: 10.1074/jbc.M116.774489

Figure 2.

Figure 2.

Mutation in putative Class I (-592SAV-) and Class II (-595CLDM-) internal PBMs and testing of their NHERF2 binding. A, one Class I PBM mutant, NHE3SAV/AA (592SAV → 592AAA), and two Class II PBM mutants, NHE3CLDM/EK (-595CLDM- → -595CEDK-) and NHE3CLDM/QA (-595CLDM- → -595CQDA-), were constructed. B, in vivo binding assays were performed. HA-tagged NHE3 constructs were immobilized by monoclonal anti-HA affinity matrix or by monoclonal anti-VSV-G antibodies immobilized on agarose as a negative control and co-precipitated with lysates from NHE3_WT, NHE3SAV/AA, NHE3CLDM/EK, and NHE3CLDM/QA in PS120/NHERF2 stable cell lines. NHE3_WT and NHE3SAV/AA precipitated NHERF2, but neither NHE3CLDM/EK nor NHE3CLDM/QA bound NHERF2. Monoclonal anti-HA antibody and polyclonal anti-NHERF2 antibody (α-2570) were used to detect HA-tagged NHE3 constructs and NHERF2, respectively. A representative experiment of three similar experiments is shown. IB, immunoblotting.