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. Author manuscript; available in PMC: 2014 Jun 27.
Published in final edited form as: Nature. 2013 Dec 12;504(7479):315–318. doi: 10.1038/nature12832

Extended Data Figure 4. Heterologous PKD1-L1 and PKD2-L1 form an ion channel.

Extended Data Figure 4

(a) Immunoprecipitation of Flag– and HA–tagged PKD1-L1 and PKD2-L1 heterologously expressed in HEK293T cells. (b) Box (± SEM) and whisker (± SD) plots of the current densities measured from PKDx-L1 family-transfected HEK cells at -100 mV (bottom) and +100 mV (top). Averages are indicated by the red lines. Statistical significance from Student's t-test comparing transfected to untransfected cells are indicated by asterisks (P-value < 0.005; n = 10-23 cells) and those comparing PKD2-L1 to the pore mutants are indicated by double asterisks (* denotes P-value < 0.005 compared to untransfected cells; ** denotes P-value < 0.005 compared to PKD 1-L1/2-L1 transfected cells; n= 9-11 cells). (c) An alignment of the PKD2-L1 and PKD2 (polycystin 2) pore helix and selectivity filter with glutamate residues D523, D525, and D530 indicated. (d) Table listing the average reversal potential change relative to the standard Na+-based extracellular solution (average खErev) and the estimated relative permeability (Px/PNa) for HEK cells transfected with PKD2-L1 alone or with PKD2-L1 and PKD1-L1 (± SEM, n= 4-6 cells).