Peptide self-assembly at the nanoscale: a challenging target for computational and experimental biotechnology

被引:125
作者
Colombo, Giorgio
Soto, Patricia
Gazit, Ehud
机构
[1] CNR, Ist Chim Riconoscimento Mol, I-20131 Milan, Italy
[2] Univ Calif Santa Barbara, Dept Chem & Biochem 9510, Santa Barbara, CA 93106 USA
[3] Tel Aviv Univ, Dept Mol Microbiol & Biotechnol, IL-66978 Tel Aviv, Israel
关键词
D O I
10.1016/j.tibtech.2007.03.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Self-assembly at the nanoscale is becoming increasingly important for the fabrication of novel supramolecular structures, with applications in the fields of nanobiotechnology and nanomedicine. Peptides represent the most favorable building blocks for the design and synthesis of nanostructures because they offer a great diversity of chemical and physical properties, they can be synthesized in large amounts, and can be modified and decorated with functional elements, which can be used in diverse applications. In this article, we review some of the most recent experimental advances in the use of nanoscale self-assembled peptide structures and the theoretical efforts aimed at understanding the microscopic determinants of their formation, stability and conformational properties. The combination of experimental observations and theoretical advances will be fundamental to fully realizing the biotechnological potential of peptide self-organization.
引用
收藏
页码:211 / 218
页数:8
相关论文
共 52 条
[1]   Responsive gels formed by the spontaneous self-assembly of peptides into polymeric beta-sheet tapes [J].
Aggeli, A ;
Bell, M ;
Boden, N ;
Keen, JN ;
Knowles, PF ;
McLeish, TCB ;
Pitkeathly, M ;
Radford, SE .
NATURE, 1997, 386 (6622) :259-262
[2]   Tau filaments from human brain and from in vitro assembly of recombinant protein show cross-β structure [J].
Berriman, J ;
Serpell, LC ;
Oberg, KA ;
Fink, AL ;
Goedert, M ;
Crowther, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (15) :9034-9038
[3]   Role of Escherichia coli curli operons in directing amyloid fiber formation [J].
Chapman, MR ;
Robinson, LS ;
Pinkner, JS ;
Roth, R ;
Heuser, J ;
Hammar, M ;
Normark, S ;
Hultgren, SJ .
SCIENCE, 2002, 295 (5556) :851-855
[4]   Protein misfolding, functional amyloid, and human disease [J].
Chiti, Fabrizio ;
Dobson, Christopher M. .
ANNUAL REVIEW OF BIOCHEMISTRY, 2006, 75 :333-366
[5]   Opposing activities protect against age-onset proteotoxicity [J].
Cohen, Ehud ;
Bieschke, Jan ;
Perciavalle, Rhonda M. ;
Kelly, Jeffery W. ;
Dillin, Andrew .
SCIENCE, 2006, 313 (5793) :1604-1610
[6]   Solvent and mutation effects on the nucleation of amyloid β-protein folding [J].
Cruz, L ;
Urbanc, B ;
Borreguero, JM ;
Lazo, ND ;
Teplow, DB ;
Stanley, HE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (51) :18258-18263
[7]   β-hairpin conformation of fibrillogenic peptides:: Structure and α-β transition mechanism revealed by molecular dynamics simulations [J].
Daidone, I ;
Simona, F ;
Roccatano, D ;
Broglia, RA ;
Tiana, G ;
Colombo, G ;
Di Nola, A .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2004, 57 (01) :198-204
[8]   De novo designed peptide-based amyloid fibrils [J].
de la Paz, ML ;
Goldie, K ;
Zurdo, J ;
Lacroix, E ;
Dobson, CM ;
Hoenger, A ;
Serrano, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (25) :16052-16057
[9]   Sequence dependence of amyloid fibril formation: Insights from molecular dynamics simulations [J].
de la Paz, ML ;
de Mori, GMS ;
Serrano, L ;
Colombo, G .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 349 (03) :583-596
[10]   All-atom folding simulations of the villin headpiece from stochastically selected coarse-grained structures [J].
De Mori, GMS ;
Micheletti, C ;
Colombo, G .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (33) :12267-12270