RT Journal Article
SR Electronic
T1 The C Terminus of the Human Nicotinic α4β2 Receptor Forms a Binding Site Required for Potentiation by an Estrogenic Steroid
JF The Journal of Neuroscience
JO J. Neurosci.
FD Society for Neuroscience
SP 6561
OP 6568
DO 10.1523/JNEUROSCI.21-17-06561.2001
VO 21
IS 17
A1 Paradiso, Ken
A1 Zhang, Jessie
A1 Steinbach, Joe Henry
YR 2001
UL http://www.jneurosci.org/content/21/17/6561.abstract
AB In addition to actions mediated by changes in gene expression, steroids can directly modulate several transmitter-gated and voltage-gated ion channels. Despite numerous studies showing that steroids enhance or reduce ion channel activity, the site(s) that mediates steroid recognition is not known. To identify the regions in which steroids bind and affect ion channel activity, we have taken advantage of the observation that human α4β2 neuronal nicotinic receptors are potentiated by an estrogen steroid, 17β-estradiol, whereas a rat α4β2 receptor is not. Mutations indicate that a sequence (AGMI) at the end of the C terminus of the human α4 subunit forms a binding site required for 17β-estradiol potentiation. In contrast, ethynyl β-estradiol (an oral contraceptive) potentiates both human and rat α4β2 receptors. A single tryptophan in the C terminus of both the rat and the human α4 subunit is sufficient for potentiation by ethynyl β-estradiol, probably through a π–π interaction. Mutation of this tryptophan eliminates the ability of ethynyl β-estradiol to potentiate rat receptors. However, in human receptors it was necessary to mutate both the AGMI sequence and the tryptophan to eliminate potentiation by ethynyl β-estradiol. The findings that β-estradiol requires the AGMI sequence but that a single C-terminal tryptophan is sufficient for potentiation by ethynyl β-estradiol indicate that the C terminus forms a binding site for these steroids. The binding site(s) for block appears to differ from those involved in potentiation because the C-terminal sequence does not affect block by steroids such as progesterone, and progesterone does not competitively inhibit potentiation.