Validation of selected binding partners of FOSL1 and FOSL2 (A,B)
FOSL1 (panel A) and FOSL2 (panel B) protein was immunoprecipitated
from 72 h-cultured Th17 cells and western blotting was used to confirm
their MS-identified interactions with SIRT-1, JUNB, RUNX1, and JUN.
Blots depict lanes for total lysate (input), control IgG IP, and FOSL1/FOSL2
IP. Figures show representative blots for two or three biological
replicates (see Figure S5 for all the replicates).
(C,D) Volcano plots show selected binding partners of FOSL1 (panel
C) and FOSL2 (panel D) that were validated by PRM-MS analysis. Data
are representative of three biological replicates. The plots were
extracted from Skyline.