Wells J A
Department of Protein Engineering, Genentech, Inc., South San Francisco, CA 94080.
Curr Opin Cell Biol. 1994 Apr;6(2):163-73. doi: 10.1016/0955-0674(94)90132-5.
Most single-pass transmembrane receptors undergo a change in oligomeric state upon hormone binding. Recent mutational, biophysical and structural studies of the human growth hormone and tumor necrosis factor receptor complexes have revealed much about the mechanisms and molecular bases for binding and oligomerization. Principles learned from these examples and others should apply to many other hormone-receptor complexes.
大多数单次跨膜受体在与激素结合后会发生寡聚状态的改变。近期对人生长激素和肿瘤坏死因子受体复合物的突变、生物物理及结构研究,已揭示了许多关于结合和寡聚化的机制及分子基础。从这些例子及其他例子中学到的原理应适用于许多其他激素 - 受体复合物。