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Formation of peptide layers and adsorption mechanisms on a negatively charged cation-exchange membrane

机译:带负电荷阳离子交换膜上的肽层的形成和吸附机制

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Graphical abstractDisplay OmittedAbstractPolypeptide/solid charged surface interactions are omnipresent in the biomedical and biochemical fields. The present study aimed to understand the adsorption mechanisms of a cation-exchange membrane (CEM) by a well-characterized peptide mixture at three different pH values. Results demonstrated that fouling was important at pH 6, twice lower at pH 2 and negligible at pH 10. At pH 6, ALPMHIR and TKIPAVFK sequences firstly established electrostatic interactions with the negative CEM charges (SO3?) through their positive K and R residues (NH3+) creating a first nanolayer. Secondly, peptide/peptide interactions occurred through their respective hydrophobic residues creating a second nanolayer. At pH 2, VLVLDTDYK and IDALNENK sequences interacted only electrostatically and that in a lower proportion since at acidic pH values, most of the CEM charges would be protonated and uncharged (HSO3) and then limit the potential electrostatic interactions. In addition, the sequences of peptides interacting at pH 2 and 6 were different. This was explained by their structure in terms of residue nature and position in the sequence. At pH 10, no fouling was observed due to the lack of positive peptide charges. To th
机译:<![cdata [ 图形摘要 显示省略 抽象 多肽/固体带电表面相互作用是生物医学和生物化学领域的全部普遍存器。本研究旨在在三种不同pH值下了解阳离子交换膜(CEM)的吸附机制。结果表明,污染在pH6的污染是重要的,pH 2下降两次,pH 10忽略不计。在pH6,AlPMHIR和TKIPAVFK序列首先与负CEM电荷建立静电相互作用(SO 3 )通过它们的正k和r残留物(nh 3 + )创建第一纳米层。其次,通过其各自的疏水残基发生肽/肽相互作用,其产生第二纳米层。在pH2,VLVLDTDYK和IDALNENK序列仅在静电相互作用,并且在酸性pH值下较低的比例,大部分CEM电荷都是质子化的,并且不带电(HSO 3 )然后限制潜在的静电相互作用。另外,在pH 2和6处相互作用的肽的序列是不同的。这是通过它们在序列中残留性质和位置方面的结构解释的。在pH10,由于缺乏阳性肽电荷,没有观察到污垢。到了

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