Jackson F R, Wilson S D, Strichartz G R, Hall L M
Nature. 1984;308(5955):189-91. doi: 10.1038/308189a0.
Voltage-sensitive sodium channels have a key role in the genesis of propagated action potentials. Mutations that affect these channels might be used like specific pharmacological agents in studies of channel structure and regulation. We have found that mutations which cause a reversible, temperature-induced paralysis in the fruit fly Drosophila melanogaster often affect the voltage-sensitive sodium channel. Using 3H-saxitoxin binding to membrane preparations, we have now identified two types of presumptive sodium channel mutants. One mutation, seizurets-2 (seits-2), appears to alter saxitoxin-binding sites structurally. The second, no-action-potential (napts) (refs 5, 6), reduces the number of saxitoxin-binding sites, but appears not to alter the receptor structure.
电压敏感钠通道在动作电位的产生过程中起关键作用。影响这些通道的突变可像特定的药理学试剂一样用于通道结构和调节的研究。我们发现,在果蝇中引起可逆的、温度诱导麻痹的突变常常影响电压敏感钠通道。利用³H-石房蛤毒素与膜制剂的结合,我们现已鉴定出两类假定的钠通道突变体。一种突变,即癫痫发作2(seits-2),似乎在结构上改变了石房蛤毒素结合位点。第二种,即无动作电位(napts)(参考文献5、6),减少了石房蛤毒素结合位点的数量,但似乎并未改变受体结构。