寡肽
肽
纳米技术
差向异构体
序列(生物学)
材料科学
纳米结构
杂质
组合化学
肽序列
氨基酸
自组装
软质材料
立体化学
化学
生物化学
有机化学
基因
作者
Yanyao Wang,Ravi R. Sonani,Libby J. Marshall,Simona Bianco,Karen E. Marshall,Alice Pincham,Honghui Yang,Louise C. Serpell,Annela M. Seddon,Edward H. Egelman,Andrew R. Thomson,Dave J. Adams
出处
期刊:Small
[Wiley]
日期:2025-09-02
卷期号:21 (42): e07714-e07714
标识
DOI:10.1002/smll.202507714
摘要
Abstract The self‐assembly of short peptides into defined nanostructures is one method for preparing soft materials and gels. Indeed, many useful materials can be prepared by the self‐assembly of oligopeptides. The design rules around such peptides are relatively established, and they assume well‐defined and pure materials. In many cases, however, the purity of the peptide is less than 95%, and the ability of likely impurities to self‐assemble is an open question. Here, the self‐assembly of the gel‐forming octapeptide FEFEFKFK and two analogues, EFEFKFK and FEFEfKFK, is discussed to examine the effect of an amino acid deletion and of epimerization at one position. Both the truncated peptide and epimerized peptide can still form gels. Mixing these peptides with the parent FEFEFKFK leads to the formation of new, but different, self‐assembled structures. This has direct implications for the understanding of the necessary design rules for self‐assembly regarding the influence of potential impurity in these systems, as well as demonstrating that much remains to be learned about sequence to structure relationships in self‐assembling peptide systems.
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