Preserving Structurally Labile Peptide Nanosheets After Molecular Functionalization of the Self-Assembling Peptides

被引:17
作者
Chen, Xin [1 ]
Xia, Cai [1 ]
Guo, Pan [1 ]
Wang, Chenru [1 ]
Zuo, Xiaobing [2 ]
Jiang, Yun-Bao [1 ]
Jiang, Tao [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, MOE Key Lab Spectrochem Anal & Instrumentat, Xiamen 361005, Peoples R China
[2] Argonne Natl Lab, Xray Sci Div, Lemont, IL 60439 USA
基金
中国国家自然科学基金;
关键词
Molecular Functionalization; Nanosheet; Peptide Self-Assembly; Staggered Assembly; COILED-COIL; CELL-ADHESION; STABILITY; PLASTICITY; PROTEINS; NANOFIBRILS; COPOLYMERS; POLYMERS; DISPLAY; DESIGN;
D O I
10.1002/anie.202315296
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A significant challenge in creating supramolecular materials is that conjugating molecular functionalities to building blocks often results in dissociation or undesired morphological transformation of their assemblies. Here we present a facile strategy to preserve structurally labile peptide assemblies after molecular modification of the self-assembling peptides. Sheet-forming peptides are designed to afford a staggered alignment with the segments bearing chemical modification sites protruding from the sheet surfaces. The staggered assembly allows for simultaneous separation of attached molecules from each other and from the underlying assembly motifs. Strikingly, using PEGs as the external molecules, PEG400- and PEG700-peptide conjugates directly self-associate into nanosheets with the PEG chains localized on the sheet surfaces. In contrast, the sheet formation based on in-register lateral packing of peptides does not recur upon the peptide PEGylation. This strategy allows for fabrication of densely modified assemblies with a variety of molecules, as demonstrated using biotin (hydrophobic molecule), c(RGDfK) (cyclic pentapeptide), and nucleic acid aptamer (negatively charged ssDNA). The staggered co-assembly also enables extended tunability of the amount/density of surface molecules, as exemplified by screening ligand-appended assemblies for cell targeting. This study paves the way for functionalization of historically challenging fragile assemblies while maintaining their overall morphology. We present a unique way to preserve structurally labile nanosheets after conjugation of a variety of molecules to the self-assembling peptides. The sheet-forming peptides afford a staggered alignment for simultaneous separation of external molecules from each other and from the underlying assembly motifs. This strategy allows the functionalization of historically challenging fragile assemblies while maintaining their overall morphology.image
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页数:8
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