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. 2020 Mar 17;295(17):5717–5736. doi: 10.1074/jbc.RA119.011946

Table 1.

Activation of PLCγ2 by catalytically-inert BTK is not limited to PLCγ2S707Y but is also observed for other PLCγ2 variants mediating ibrutinib resistance in CLL cells

COS-7 cells were transfected as indicated with 150 ng/well vector encoding WT PLCγ2 (PLCγ2WT); 50 ng/well vector encoding the PLCγ2 variants D334H, R665W, S707Y, S707F, L845F, D993H, and M1141R; 15 ng of vector encoding PLCγ2S707P; and 100 ng/well of vector encoding BTKWT or BTK variants K430R, E41K, or E41K/K430R. The ratios of the PLC activities determined in the presence of BTKE41K/K430R and BTKE41K are specified in the right column. The data depicted in the table show representative results from three independent experiments each as mean values of three technical replicates.

BTK Inositol phosphate formation
Ratio (E41K/K430R:E41K)
Control WT K430R E41K E41K/K430R
cpm %
PLCγ2WT 67 86 67 2358 121 5.2
PLCγ2D334H 40 1097 236 10089 4390 43.5
PLCγ2R665W 42 374 138 4420 1956 44.3
PLCγ2S707Y 231 1998 713 17442 8132 46.6
PLCγ2S707F 464 2561 1488 20150 11215 55.7
PLCγ2S707P 728 2991 2563 17734 11584 65.3
PLCγ2L845F 219 1660 455 8937 9668 108.2
PLCγ2D993H 702 3604 1888 10808 7892 73.0
PLCγ2M1141R 1966 5858 5395 14268 14187 99.4