Anand R, Peng X, Lindstrom J
Department of Neuroscience, University of Pennsylvania, Philadelphia 19104-607.
FEBS Lett. 1993 Jul 26;327(2):241-6. doi: 10.1016/0014-5793(93)80177-v.
Sucrose gradient analysis of chick acetylcholine receptor (AChR) alpha 7 subunits expressed in oocytes indicates that they form pharmacologically active homomers of the same size as native alpha 7 AChRs, a size compatible with a complex of five alpha 7 subunits. By immunoisolating the [35S]methionine-labeled alpha 7 subunits we also demonstrate that they do not appear to assemble with endogenous Xenopus AChR subunits. Pharmacological characterization of detergent-solubilized brain alpha 7 AChRs and alpha 7 homomers reveals that they have similar but nonidentical properties. The pharmacological difference is most accentuated for cytisine (approximately 50-fold). Thus, at least in E18 chicken brain, most or all of the native alpha 7 AChRs do not appear to be homomeric.
对在卵母细胞中表达的鸡乙酰胆碱受体(AChR)α7亚基进行蔗糖梯度分析表明,它们形成了与天然α7 AChRs大小相同的具有药理学活性的同聚体,该大小与五个α7亚基的复合物相符。通过免疫分离[35S]甲硫氨酸标记的α7亚基,我们还证明它们似乎不会与内源性非洲爪蟾AChR亚基组装。对去污剂溶解的脑α7 AChRs和α7同聚体的药理学特性进行表征发现,它们具有相似但不完全相同的特性。对于金雀花碱,药理学差异最为明显(约50倍)。因此,至少在E18鸡脑中,大多数或所有天然α7 AChRs似乎都不是同聚体。