Gaucher J F, Ménez R, Arnoux B, Pusset J, Ducruix A
Laboratoire d'Enzymologie et de Biochimie Structurales, UPR 9063 CNRS, 91198 Gif-sur-Yvette, France.
Eur J Biochem. 2000 Mar;267(5):1323-9. doi: 10.1046/j.1432-1327.2000.01099.x.
A previous mutational analysis of erabutoxin a (Ea), a curaremimetic toxin from sea snake venom, showed that the substitutions S8G and S8T caused, respectively, 176-fold and 780-fold affinity decreases for the nicotinic acetylcholine receptor (AchR). In view of the fact that the side-chain of Ser8 is buried in the wild-type toxin, we wondered whether these affinity changes reflect a direct binding contribution of S8 to the receptor and/or conformational changes that could have occurred in Ea as a result of the introduced mutations. To approach this question, we solved X-ray structures of the two mutants S8G and S8T at high resolution (0.18 nm and 0.17 nm, with R factors of 18.0% and 17.9%, respectively). The data show that none of the mutations significantly modified the toxin structure. Even within the site where the toxin binds to the receptor the backbone conformation remained unchanged. Therefore, the low affinities of the mutants S8T and S8G cannot be explained by a large conformational change of the toxin structure. Although we cannot exclude the possibility that undetectable structural changes have occurred in the toxin mutants, our data support the view that, although buried between loop I and II, S8 is part of the functional epitope of the toxin.
先前对海蛇毒中一种箭毒样毒素—— erabutoxin a(Ea)的突变分析表明,S8G和S8T替换分别导致对烟碱型乙酰胆碱受体(AchR)的亲和力下降了176倍和780倍。鉴于Ser8的侧链在野生型毒素中是埋藏的,我们想知道这些亲和力变化是否反映了S8对受体的直接结合贡献和/或由于引入的突变可能在Ea中发生的构象变化。为了解决这个问题,我们以高分辨率(0.18 nm和0.17 nm,R因子分别为18.0%和17.9%)解析了两个突变体S8G和S8T的X射线结构。数据表明,没有一个突变显著改变毒素结构。即使在毒素与受体结合的位点内,主链构象也保持不变。因此,突变体S8T和S8G的低亲和力不能用毒素结构的大构象变化来解释。虽然我们不能排除毒素突变体中发生了不可检测的结构变化的可能性,但我们的数据支持这样一种观点,即尽管S8埋藏在环I和环II之间,但它是毒素功能表位的一部分。