Inhibition of Protein Kinase Cα by Dequalinium Analogues: Dependence on Linker Length and Geometry
作者:Donghui Qin、Regina Sullivan、William F. Berkowitz、Robert Bittman、Susan A. Rotenberg
DOI:10.1021/jm990340z
日期:2000.4.6
Analogues of a bipartite compound, dequalinium (DECA) (quinolinium, 1,1'-(1,10-decanediyl)bis(4-amino-2-methyl diiodide)), were tested for inhibition of protein kinase C alpha (PKC alpha). In vitro assays of monomeric and dimeric analogues support a model in which DECA inhibits PKC alpha by an obligatory two-point contact, a unique mechanism among PKC inhibitors. The presence of unsaturation in the center of the C-10-alkyl linker produced geometric isomers with different inhibitory potencies: cis IC50 = 52 +/- 12 mu M and trans IC50 = 12 +/- 3 mu M, where the trans isomer was equipotent to that of the saturated C-10-DECA. DECA analogues with longer, saturated linkers (C-12, C-14, or C-16) exhibited enhanced inhibitory potencies which reached a plateau with the C-14-linker (IC50 = 2.6 +/- 0.2 mu M) Metastatic melanoma cells treated with 250 nM C-12-, C-14-, or C-16-DECA and irradiated with long-wave UV light (which causes irreversible inhibition of PKC alpha by DECA) confirmed the linker-dependent inhibition of intracellular PKC alpha activity.