Creating nanocavities of tunable sizes: Hollow helices

被引:144
作者
Gong, B [1 ]
Zeng, HQ
Zhu, J
Yuan, LH
Han, YH
Cheng, SZ
Furukawa, M
Parra, RD
Kovalevsky, AY
Mills, JL
Skrzypczak-Jankun, E
Martinovic, S
Smith, RD
Zheng, C
Szyperski, T
Zeng, XC
机构
[1] SUNY Buffalo, Dept Chem, Buffalo, NY 14260 USA
[2] Univ Nebraska, Dept Chem, Lincoln, NE 68588 USA
[3] Univ Toledo, Dept Chem, Toledo, OH 43606 USA
[4] Pacific NW Natl Lab, Environm & Mol Sci Lab, Richland, WA 99352 USA
[5] No Illinois Univ, Dept Chem, De Kalb, IL 60115 USA
关键词
D O I
10.1073/pnas.162277099
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
A general strategy for creating nanocavities with tunable sizes based on the folding of unnatural oligomers is presented. The backbones of these oligomers are rigidified by localized, three-center intramolecular hydrogen bonds, which lead to well-defined hollow helical conformations. Changing the curvature of the oligomer backbone leads to the adjustment of the interior cavity size. Helices with interior cavities of 10 Angstrom to >30 Angstrom across, the largest thus far formed by the folding of unnatural foldamers, are generated. Cavities of these sizes are usually seen at the tertiary and quaternary structural levels of proteins. The ability to tune molecular dimensions without altering the underlying topology is seen in few natural and unnatural foldamer systems.
引用
收藏
页码:11583 / 11588
页数:6
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