芋螺毒素
突变体
乙酰胆碱受体
烟碱激动剂
效力
亚科
IC50型
化学
药理学
生物
立体化学
受体
生物化学
体外
毒液
基因
作者
Jianying Dong,Panpan Zhang,Junjie Xie,Ting Xie,Xiaopeng Zhu,Dongting Zhangsun,Jinpeng Yu,Sulan Luo
出处
期刊:Marine Drugs
[Multidisciplinary Digital Publishing Institute]
日期:2023-05-01
卷期号:21 (5): 286-286
被引量:4
摘要
α4/6-conotoxin TxID, which was identified from Conus textile, simultaneously blocks rat (r) α3β4 and rα6/α3β4 nicotinic acetylcholine receptors (nAChRs) with IC50 values of 3.6 nM and 33.9 nM, respectively. In order to identify the effects of loop2 size on the potency of TxID, alanine (Ala) insertion and truncation mutants were designed and synthesized in this study. An electrophysiological assay was used to evaluate the activity of TxID and its loop2-modified mutants. The results showed that the inhibition of 4/7-subfamily mutants [+9A]TxID, [+10A]TxID, [+14A]TxID, and all the 4/5-subfamily mutants against rα3β4 and rα6/α3β4 nAChRs decreased. Overall, ala-insertion or truncation of the 9th, 10th, and 11th amino acid results in a loss of inhibition and the truncation of loop2 has more obvious impacts on its functions. Our findings have strengthened the understanding of α-conotoxin, provided guidance for further modifications, and offered a perspective for future studies on the molecular mechanism of the interaction between α-conotoxins and nAChRs.
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