In vitro fluorescence anisotropy analysis of the interaction of full-length SRC1a with estrogen receptors α and β supports an active displacement model for coregulator utilization

Binding of full-length P160 coactivators to hormone response element-steroid receptor complexes has been difficult to investigate in vitro. Here, we report a new application of our recently described fluorescence anisotropy microplate assay to investigate binding and dissociation of full-length steroid receptor coactivator-1a (SRC1a) from full-length estrogen receptor alpha (ER alpha) or estrogen receptor beta(ER beta) bound to a fluorescein-labeled (fl) estrogen response element (ERE). SRC1a exhibited slightly higher affinity binding to flERE(.)ER beta than to flERE(.)ER beta. Binding of SRC1a to flERE(.)ER alpha and to flERE(.)ER alpha was 17 beta-estradiol (E-2)-dependent and was nearly absent when ICI 182,780, raloxifene, or 4- hydroxytamoxifen were bound to the ERs. SRC1a binds to flERE E-.(2)-ER alpha and flERE(.)E(2)-ER beta complexes with a t(1/2) of 15 - 20 s. Short LXXLL-containing nuclear receptor (NR) box peptides from P160 coactivators competed much better for SRC1a binding to flERE(.)E(2)-ER than an NR box peptide from TRAP220. However, similar to 40-250-fold molar excess of the P160 NR box peptides was required to inhibit SRC1a binding by 50%. This suggests that whereas the NR box region is a primary site of interaction between SRC1a and (EREE2)-E-.-ER additional contacts between the coactivator and the ligand-receptor-DNA complex make substantial contributions to overall affinity. Increasing amounts of NR box peptides greatly enhanced the rate of dissociation of SRC1a from preformed flERE(.)E(2)-ER complexes. The data support a model in which coactivator exchange is facilitated by active displacement and is not simply the result of passive dissociation and replacement. It also shows that an isolated coactivator exhibits an inherent capacity for rapid exchange.