Self-assembled peptide fibers from valylvaline bola-amphiphiles by a parallel β-sheet network

被引:54
作者
Kogiso, M [1 ]
Okada, Y [1 ]
Hanada, T [1 ]
Yase, K [1 ]
Shimizu, T [1 ]
机构
[1] Natl Inst Mat & Chem Res, Tsukuba, Ibaraki 3058565, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2000年 / 1475卷 / 03期
关键词
bola-amphiphile; peptide fiber; L-valyl-L-valine; self-assembly; beta-sheet; FT-IR spectroscopy;
D O I
10.1016/S0304-4165(00)00088-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of dipeptide-based bola-amphiphiles, bis(N-alpha-amide-L-valyl-L-valine) 1, n-alkane dicarboxylate (n = 4-12), have been synthesized. The bola-amphiphiles with n = 4 and 6 self-assembled to form crystalline solids in water, whereas those with n = 7-12 produced peptide fibers. FT-IR spectroscopy and X-ray diffraction patterns revealed that the peptide fibers have parallel-type beta-sheet networks between the valylvaline units. FT-IR deconvolution study of carboxyl regions indicated that these crystalline solids and peptide fibers are stabilized by interlayer bifurcated and intralayer lateral hydrogen-bond networks between the end carboxylic acid groups, respectively. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:346 / 352
页数:7
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