Peptide Design and Self-assembly into Targeted Nanostructure and Functional Materials

被引:165
|
作者
Sinha, Nairiti J. [1 ]
Langenstein, Matthew G. [1 ]
Pochan, Darrin J. [1 ]
Kloxin, Christopher J. [1 ,2 ]
Saven, Jeffery G. [3 ]
机构
[1] Univ Delaware, Dept Mat Sci & Engn, Newark, DC 19716 USA
[2] Univ Delaware, Dept Chem & Biomol Engn, Newark, DC 19716 USA
[3] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
关键词
ALPHA-HELICAL PEPTIDE; COILED-COIL PEPTIDE; ANGLE NEUTRON-SCATTERING; NOVO PROTEIN DESIGN; RATIONAL DESIGN; COMPUTATIONAL DESIGN; POLYPEPTIDE VESICLES; SECONDARY STRUCTURE; BETA-SHEET; DNA;
D O I
10.1021/acs.chemrev.1c00712
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Peptides have been extensively utilized to construct nanomaterials that display targeted structure through hierarchical assembly. The self-assembly of both rationally designed peptides derived from naturally occurring domains in proteins as well as intuitively or computationally designed peptides that form beta-sheets and helical secondary structures have been widely successful in constructing nanoscale morphologies with well-defined 1-d, 2-d, and 3-d architectures. In this review, we discuss these successes of peptide self-assembly, especially in the context of designing hierarchical materials. In particular, we emphasize the differences in the level of peptide design as an indicator of complexity within the targeted self-assembled materials and highlight future avenues for scientific and technological advances in this field.
引用
收藏
页码:13915 / 13935
页数:21
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