Photoresponsive behavior of self-assembling systems by amphiphilic α-helix with azobenzene unit

被引:9
作者
Higuchi, M
Kinoshita, T
机构
[1] Natl Inst Mat & Chem Res, Dept Organ Mat, Tsukuba, Ibaraki 305, Japan
[2] Nagoya Inst Technol, Dept Mat Sci & Engn, Showa Ku, Nagoya, Aichi 466, Japan
关键词
photoresponsive amphiphilic polypeptides; self-assembly; supermolecules; photoisomerization; morphological changes;
D O I
10.1016/S1011-1344(98)00066-9
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 photoresponsive amphiphilic polypeptide composed of two amphiphilic alpha-helical polypeptides, poly[(gamma-methyl L-glutamate)-co-(L-glutamic acid)],joined with an azobenzene moiety, was prepared via the monolayer reaction method. We investigated the photoinduced changes in the aggregate structure of the polypeptide in aqueous solution. The polypeptides were soluble in aqueous solution and associated with each other to form a globular aggregate approximate to 10 nm in diameter in the dark. The globular aggregate grew into a twisted ribbon-like structure which could be observed with an optical microscope. The trans-to-cis isomerization of the azobenzene unit in the main chain induced a bending of the polypeptide rod, which resulted in a dissociation of the aggregate. In this process, the degree of disaggregation was not linear to the irradiated light intensity, i.e., the photoinduced effect appeared over a certain value of the light intensity. Such on-off deformations of the supramolecular order may be due to a native character of self-organizing systems supported by weak but cooperative intermolecular interactions. (C) 1998 Elsevier Science S.A.
引用
收藏
页码:143 / 150
页数:8
相关论文
共 40 条
[1]   SELF-ASSEMBLING HEXAMERIC HELICAL BUNDLE FORMING PEPTIDES [J].
CHIN, TM ;
BERNDT, KD ;
YANG, NCC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (06) :2279-2280
[2]  
COOPER TM, 1993, TRENDS POLYM SCI, V1, P400
[3]   THE PREPARATION OF N-CARBOXYANHYDRIDES OF ALPHA-AMINO-ACIDS USING BIS(TRICHLOROMETHYL)CARBONATE [J].
DALY, WH ;
POCHE, D .
TETRAHEDRON LETTERS, 1988, 29 (46) :5859-5862
[4]  
DRAPEAU GR, 1972, J BIOL CHEM, V247, P6720
[5]   LIPID BILAYER FIBERS FROM DIASTEREOMERIC AND ENANTIOMERIC N-OCTYLALDONAMIDES [J].
FUHRHOP, JH ;
SCHNIEDER, P ;
BOEKEMA, E ;
HELFRICH, W .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (09) :2861-2867
[6]   MOLECULAR MONOLAYER RODS AND TUBULES MADE OF ALPHA-(L-LYSINE),OMEGA-(AMINO) BOLAAMPHIPHILES [J].
FUHRHOP, JH ;
SPIROSKI, D ;
BOETTCHER, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (04) :1600-1601
[7]   SELF-ASSEMBLING ORGANIC NANOTUBES BASED ON A CYCLIC PEPTIDE ARCHITECTURE [J].
GHADIRI, MR ;
GRANJA, JR ;
MILLIGAN, RA ;
MCREE, DE ;
KHAZANOVICH, N .
NATURE, 1993, 366 (6453) :324-327
[8]   DESIGN OF AN ARTIFICIAL 4-HELIX BUNDLE METALLOPROTEIN VIA A NOVEL RUTHENIUM(II)-ASSISTED SELF-ASSEMBLY PROCESS [J].
GHADIRI, MR ;
SOARES, C ;
CHOI, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (10) :4000-4002
[9]   THE STRUCTURAL AND THERMODYNAMIC BASIS FOR THE FORMATION OF SELF-ASSEMBLED PEPTIDE NANOTUBES [J].
GHADIRI, MR ;
KOBAYASHI, K ;
GRANJA, JR ;
CHADHA, RK ;
MCREE, DE .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (01) :93-95
[10]   ARTIFICIAL TRANSMEMBRANE ION CHANNELS FROM SELF-ASSEMBLING PEPTIDE NANOTUBES [J].
GHADIRI, MR ;
GRANJA, JR ;
BUEHLER, LK .
NATURE, 1994, 369 (6478) :301-304