Rapid discovery of self-assembling peptides with one-bead one-compound peptide library

被引:41
作者
Yang, Pei-Pei [1 ]
Li, Yi-Jing [1 ,2 ]
Cao, Yan [3 ]
Zhang, Lu [4 ]
Wang, Jia-Qi [1 ]
Lai, Ziwei [3 ]
Zhang, Kuo [1 ,2 ]
Shorty, Diedra [4 ]
Xiao, Wenwu [4 ]
Cao, Hui [2 ]
Wang, Lei [1 ]
Wang, Hao [1 ,5 ]
Liu, Ruiwu [4 ]
Lam, Kit S. [4 ,6 ]
机构
[1] Natl Ctr Nanosci & Technol NCNST, CAS Key Lab Biomed Effects Nanomat & Nanosa, CAS Ctr Excellence Nanosci, 11 Beiyitiao, Beijing, Peoples R China
[2] Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Dept Mat Phys & Chem, Beijing, Peoples R China
[3] Shenzhen Univ, Inst Adv Study, Shenzhen, Guangdong, Peoples R China
[4] Univ Calif Davis, UC Davis NCI Designated Comprehens Canc Ctr, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
[5] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelectron Engn, Beijing, Peoples R China
[6] Univ Calif Davis, Sch Med, Dept Internal Med, Div Hematol & Oncol, Sacramento, CA 95817 USA
基金
中国国家自然科学基金;
关键词
NANOPARTICLES; NANOSTRUCTURES; MOLECULES; ARREST; WATER; TOOL;
D O I
10.1038/s41467-021-24597-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Self-assembling peptides have shown tremendous potential in the fields of material sciences, nanoscience, and medicine. Because of the vast combinatorial space of even short peptides, identification of self-assembling sequences remains a challenge. Herein, we develop an experimental method to rapidly screen a huge array of peptide sequences for self-assembling property, using the one-bead one-compound (OBOC) combinatorial library method. In this approach, peptides on beads are N-terminally capped with nitro-1,2,3-benzoxadiazole, a hydrophobicity-sensitive fluorescence molecule. Beads displaying self-assembling peptides would fluoresce under aqueous environment. Using this approach, we identify eight pentapeptides, all of which are able to self-assemble into nanoparticles or nanofibers. Some of them are able to interact with and are taken up efficiently by HeLa cells. Intracellular distribution varied among these non-toxic peptidic nanoparticles. This simple screening strategy has enabled rapid identification of self-assembling peptides suitable for the development of nanostructures for various biomedical and material applications. Self-assembling peptides have a range of potential applications but developing self-assembling sequences can be challenging. Here, the authors report on a one-bead one-compound combinatorial library where fluorescence is used to detect the potential for self-assembly and identified candidates are evaluated.
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页数:8
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