Lei Ying, Hagen Guy M, Smith Steven M L, Liu Jinging, Barisas George, Roess Deborah A
Cell and Molecular Biology Program, Colorado State University, Fort Collins, CO 80523, United States.
Mol Cell Endocrinol. 2007 Jan 2;260-262:65-72. doi: 10.1016/j.mce.2005.11.046. Epub 2006 Oct 11.
Several naturally occurring mutations in human luteinizing hormone receptors (LHR) at position 578 are associated with constitutive activation of the receptor. To determine whether human LHRs that signal in the absence of ligand are self-associated, fluorescence resonance energy transfer (FRET) between receptors was evaluated. Values for FRET between wild type LHR in the absence of ligand were less than 1% and increased significantly to over 11% after exposure to hCG. Constitutively active receptors exhibited 11-15% FRET efficiency in the absence of hormone and these values did not change with hCG treatment. A large fraction of constitutively active LHR-D578H receptors were also associated with so-called plasma membrane rafts. Disruption of these membrane microdomains reduced FRET efficiency but did not affect signalling through cAMP. Thus, in the absence of ligand, constitutively active receptors are self-associated and located in high buoyancy membrane fractions, both characteristics of the hormone-treated wild type receptor.
人类促黄体生成素受体(LHR)第578位的几种天然发生的突变与受体的组成型激活有关。为了确定在无配体情况下发出信号的人类LHR是否自缔合,评估了受体之间的荧光共振能量转移(FRET)。在无配体情况下,野生型LHR之间的FRET值小于1%,在暴露于hCG后显著增加至超过11%。组成型激活的受体在无激素情况下表现出11 - 15%的FRET效率,并且这些值在hCG处理后没有变化。很大一部分组成型激活的LHR - D578H受体也与所谓的质膜筏相关。这些膜微区的破坏降低了FRET效率,但不影响通过cAMP的信号传导。因此,在无配体情况下,组成型激活的受体是自缔合的,并且位于高浮力膜组分中,这两个特征与激素处理后的野生型受体相同。