肽
化学
合理设计
超分子化学
劈理(地质)
两亲性
自组装
生物物理学
蛋白酵素
超分子组装
单体
组合化学
酶
纳米技术
分子
生物化学
共聚物
聚合物
材料科学
生物
有机化学
复合材料
断裂(地质)
作者
Yi‐An Lin,Yu‐Chuan Ou,Andrew G. Cheetham,Honggang Cui
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2014-03-10
卷期号:15 (4): 1419-1427
被引量:70
摘要
One-dimensional nanostructures formed by self-assembly of small molecule peptides have been extensively explored for use as biomaterials in various biomedical contexts. However, unlike individual peptides that can be designed to be specifically degradable by enzymes/proteases of interest, their self-assembled nanostructures, particularly those rich in β-sheets, are generally resistant to enzymatic degradation because the specific cleavage sites are often embedded inside the nanostructures. We report here on the rational design of β-sheet rich supramolecular filaments that can specifically dissociate into less stable micellar assemblies and monomers upon treatment with matrix metalloproteases-2 (MMP-2). Through linkage of an oligoproline segment to an amyloid-derived peptide sequence, we first synthesized an amphiphilic peptide that can undergo a rapid morphological transition in response to pH variations. We then used MMP-2 specific peptide substrates as multivalent cross-linkers to covalently fix the amyloid-like filaments in the self-assembled state at pH 4.5. Our results show that the cross-linked filaments are stable at pH 7.5 but gradually break down into much shorter filaments upon cleavage of the peptidic cross-linkers by MMP-2. We believe that the reported work presents a new design platform for the creation of amyloid-like supramolecular filaments responsive to enzymatic degradation.
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