首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Primary structure of Euplotes raikovi pheromones: comparison of five sequences of pheromones from cells with variable mating interactions.
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Primary structure of Euplotes raikovi pheromones: comparison of five sequences of pheromones from cells with variable mating interactions.

机译:Euplotes raikovi信息素的一级结构:来自具有可变交配相互作用的细胞的信息素的五个序列的比较。

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摘要

The amino acid sequences of five pheromones, Er-2, Er-3, Er-9, Er-11, and Er-20, secreted by cells of different mating types of the ciliated protozoa Euplotes raikovi, have been determined by automated Edman analyses of the whole proteins and germane fragments. In each case, the molecular mass was determined by plasma desorption or laser desorption mass spectrometry and was in excellent agreement with the calculated values. Where available, the determined sequences were also in accord with the corresponding segments of the precursor molecules predicted from relevant nucleic acid sequences. Of the five, two were found to be identical (Er-2 and Er-9) and one (Er-3) was identical to a pheromone previously sequenced (Er-1), even though mating pair formation was found to take place (although to a limited extent) when cells secreting those pheromones were combined in a mixture. Comparison of the five unique sequences suggested a closer relationship between Er-1 (Er-3) and Er-10 and between Er-11 and Er-20 (44% and 56% identity, respectively) than was generally observed among the other members. This pairing was also supported by hydrophobicity analyses. Interestingly, Er-20 cannot, as a rule, induce cell union in any of the other cell types, including cells secreting Er-11, despite the fact that Er-20 and Er-11 are the most similar of the five unique sequences. Thus sequence identity and secondary structure profiles are not a good indicator of biological relatedness as manifested in heterologous receptor interaction.
机译:通过自动埃德曼分析确定了纤毛原生动物Eupplotes raikovi不同交配类型的细胞分泌的五个信息素Er-2,Er-3,Er-9,Er-11和Er-20的氨基酸序列。整个蛋白质和锗烷片段。在每种情况下,分子量都是通过等离子体解吸或激光解吸质谱法测定的,与计算值非常吻合。在可获得的情况下,确定的序列也与根据相关核酸序列预测的前体分子的相应片段一致。在这五种中,即使发现形成配对,也发现其中两种是相同的(Er-2和Er-9),而一种(Er-3)与先前测序的信息素(Er-1)相同( (在有限的程度上))将分泌这些信息素的细胞混合在一起。五个独特序列的比较表明,Er-1(Er-3)和Er-10之间以及Er-11和Er-20之间的关系比其他成员之间的关系更紧密(分别为44%和56%) 。疏水性分析也支持该配对。有趣的是,尽管Er-20和Er-11是五个独特序列中最相似的事实,但Er-20通常不能诱导任何其他细胞类型的细胞结合,包括分泌Er-11的细胞。因此,如异源受体相互作用中所示,序列同一性和二级结构概况不是生物学相关性的良好指标。

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