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Tuning Chelation by the Surfactant-Like Peptide A6H Using Predetermined pH Values

机译:使用预定的pH值调节表面活性剂样肽A6H的螯合

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We examine the self-assembly of a peptide A6H comprising a hexa-alanine sequence A6 with a histidine (H) "head group", which chelates Zn~(2+) cations. We study the self-assembly of A6H and binding of Zn~(2+) ions in ZnCl2 solutions, under acidic and neutral conditions. A6H self-assembles into nanotapes held together by a β-sheet structure in acidic aqueous solutions. By dissolving A6H in acidic ZnCl2 solutions, the carbonyl oxygen atoms in A6H chelate the Zn~(2+) ions and allow for β-sheet formation at lower concentrations, consequently reducing the onset concentration for nanotape formation. A6H mixed with water or ZnCl2 solutions under neutral conditions produces short sheets or pseudocrystalline tapes, respectively. The imidazole ring of A6H chelates Zn~(2+) ions in neutral solutions. The internal structure of nanosheets and pseudocrystalline sheets in neutral solutions is similar to the internal structure of A6H nanotapes in acidic solutions. Our results show that it is possible to induce drarnatic changes in the self-assembly and chelation sites of A6H by changing the pH of the solution. However, it is likely that the amphiphilic nature of A6H determines the internal structure of the self-assembled aggregates independent from changes in chelation.
机译:我们研究了包含六丙氨酸序列A6和组氨酸(H)“头基”的肽A6H的自组装,该组氨酸螯合Zn〜(2+)阳离子。我们研究了酸性和中性条件下A6H的自组装和ZnCl2溶液中Zn〜(2+)离子的结合。 A6H在酸性水溶液中自组装成纳米带,并通过β-折叠结构将其保持在一起。通过将A6H溶解在酸性ZnCl2溶液中,A6H中的羰基氧原子螯合Zn〜(2+)离子,并允许以较低的浓度形成β-片层,从而降低了纳米带形成的起始浓度。在中性条件下将A6H与水或ZnCl2溶液混合会分别产生短片或假晶带。在中性溶液中,A6H的咪唑环螯合Zn〜(2+)离子。中性溶液中的纳米片和假晶体片的内部结构类似于酸性溶液中的A6H纳米带的内部结构。我们的结果表明,通过改变溶液的pH值可以诱导A6H的自组装和螯合位点发生剧烈变化。但是,A6H的两亲性质很可能决定了自组装聚集体的内部结构,而与螯合的变化无关。

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