由单一脂肪酸触发的二肽超分子组装中的级联相变。

IF 5.6 2区 医学 Q1 BIOPHYSICS
Kaifeng Guo , Liang Gao , Jinbo Fei
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引用次数: 0

摘要

短肽超分子组合的多样性研究取得了重大进展。然而,单刺激的可编程相位调制仍然是一个巨大的挑战。在这里,我们证明了一个二肽超分子体系经历了由单个脂肪酸触发的氢键结合和解离的顺序耦合相变。具体来说,低比脂肪酸通过氢键相互作用的重排介导了二肽超分子组装的凝胶-晶体转化。此外,高比脂肪酸通过二肽的质子化诱导晶体-溶胶转变,产生强烈的静电斥力来分裂氢键相互作用。值得注意的是,相变的级联使二肽能够从一个分散相中自发地固液分离,并以捕获和释放的方式进一步溶解在另一个分散相中。相反,单个相变不能促进这一过程。我们的工作创造了竞争途径,以实现简单的二肽超分子系统的相变整合。这有助于深入了解自然界动态复杂的生物分子凝聚体,对生物分子的高效收集具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cascade of phase transitions in a dipeptide supramolecular assembly triggered by a single fatty acid
Significant progress has been achieved with diversity of short peptide supramolecular assemblies. However, their programmable phase modulation by single stimulus remains a great challenge. Herein, we demonstrate a dipeptide supramolecular system undergoes sequentially coupled phase transitions upon hydrogen bonding association and dissociation triggered by a single fatty acid. To be specific, fatty acid at a low specific ratio mediates gel-crystal transformation of the dipeptide supramolecular assembly by rearrangement of hydrogen bonding interactions. Moreover, fatty acid at a high specific ratio induces crystal-sol transition by protonation of the dipeptide, generating strong electrostatic repulsion to cleave hydrogen bonding interactions. Remarkably, the cascade of phase transitions enables spontaneous solid-liquid separation of the dipeptide from one dispersion phase and further dissolution in another in a capture and release fashion. In contrast, it is not facilitated by individual phase transition. Our work creates competitive pathways to achieve integration of phase transitions in a simple dipeptide supramolecular system. It is useful to deeply understand the dynamic and complex biomolecular condensates in nature and with important implications for efficient collection of biomolecules.
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来源期刊
Colloids and Surfaces B: Biointerfaces
Colloids and Surfaces B: Biointerfaces 生物-材料科学:生物材料
CiteScore
11.10
自引率
3.40%
发文量
730
审稿时长
42 days
期刊介绍: Colloids and Surfaces B: Biointerfaces is an international journal devoted to fundamental and applied research on colloid and interfacial phenomena in relation to systems of biological origin, having particular relevance to the medical, pharmaceutical, biotechnological, food and cosmetic fields. Submissions that: (1) deal solely with biological phenomena and do not describe the physico-chemical or colloid-chemical background and/or mechanism of the phenomena, and (2) deal solely with colloid/interfacial phenomena and do not have appropriate biological content or relevance, are outside the scope of the journal and will not be considered for publication. The journal publishes regular research papers, reviews, short communications and invited perspective articles, called BioInterface Perspectives. The BioInterface Perspective provide researchers the opportunity to review their own work, as well as provide insight into the work of others that inspired and influenced the author. Regular articles should have a maximum total length of 6,000 words. In addition, a (combined) maximum of 8 normal-sized figures and/or tables is allowed (so for instance 3 tables and 5 figures). For multiple-panel figures each set of two panels equates to one figure. Short communications should not exceed half of the above. It is required to give on the article cover page a short statistical summary of the article listing the total number of words and tables/figures.
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