Evolving the use of peptides as components of biomaterials

被引:179
作者
Collier, Joel H. [1 ]
Segura, Tatiana [2 ]
机构
[1] Univ Chicago, Dept Surg, Chicago, IL 60637 USA
[2] Univ Calif Los Angeles, Dept Chem & Biomol Engn, Los Angeles, CA 90095 USA
关键词
Peptide; Biomaterials; Extracellular matrix; Tissue engineering; Regenerative medicine; SELF-ASSEMBLED MONOLAYERS; CHEMICAL-SYNTHESIS; CELL-ADHESION; CROSS-LINKING; HYDROGELS; FIBRONECTIN; PROTEINS; IMMOBILIZATION; SCAFFOLDS; ANCHORAGE;
D O I
10.1016/j.biomaterials.2011.02.030
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This manuscript is part of a debate on the statement that "the use of short synthetic adhesion peptides, like RGD, is the best approach in the design of biomaterials that guide cell behavior for regenerative medicine and tissue engineering". We take the position that although there are some acknowledged disadvantages of using short peptide ligands within biomaterials, it is not necessary to discard the notion of using peptides within biomaterials entirely, but rather to reinvent and evolve their use. Peptides possess advantageous chemical definition, access to non-native chemistries, amenability to de novo design, and applicability within parallel approaches. Biomaterials development programs that require such aspects may benefit from a peptide-based strategy. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4198 / 4204
页数:7
相关论文
共 102 条
[1]   Rational design of peptide-based building blocks for nanoscience and synthetic biology [J].
Armstrong, Craig T. ;
Boyle, Aimee L. ;
Bromley, Elizabeth H. C. ;
Mahmoud, Zahra N. ;
Smith, Lisa ;
Thomson, Andrew R. ;
Woolfson, Derek N. .
FARADAY DISCUSSIONS, 2009, 143 :305-317
[2]   Self-Assembly of Multidomain Peptides: Sequence Variation Allows Control over Cross-Linking and Viscoelasticity [J].
Aulisa, Lorenzo ;
Dong, He ;
Hartgerink, Jeffrey D. .
BIOMACROMOLECULES, 2009, 10 (09) :2694-2698
[3]   ARG-GLY-ASP CONSTRAINED WITHIN CYCLIC PENTAPEPTIDES - STRONG AND SELECTIVE INHIBITORS OF CELL-ADHESION TO VITRONECTIN AND LAMININ FRAGMENT-P1 [J].
AUMAILLEY, M ;
GURRATH, M ;
MULLER, G ;
CALVETE, J ;
TIMPL, R ;
KESSLER, H .
FEBS LETTERS, 1991, 291 (01) :50-54
[4]   Selection and analysis of solid-binding peptides [J].
Baneyx, Francois ;
Schwartz, Daniel T. .
CURRENT OPINION IN BIOTECHNOLOGY, 2007, 18 (04) :312-317
[5]  
Banwell EF, 2009, NAT MATER, V8, P596, DOI [10.1038/NMAT2479, 10.1038/nmat2479]
[6]   Reactivation of the p53 tumor suppressor pathway by a stapled p53 peptide [J].
Bernal, Federico ;
Tyler, Andrew F. ;
Korsmeyer, Stanley J. ;
Walensky, Loren D. ;
Verdine, Gregory L. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (09) :2456-+
[7]   Hydrocarbon double-stapling remedies the proteolytic instability of a lengthy peptide therapeutic [J].
Bird, Gregory H. ;
Madani, Navid ;
Perry, Alisa F. ;
Princiotto, Amy M. ;
Supko, Jeffrey G. ;
He, Xiaoying ;
Gavathiotis, Evripidis ;
Sodroski, Joseph G. ;
Walensky, Loren D. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (32) :14093-14098
[8]   Segment coupling to a highly hindered N-terminal, alamethicin-related α-aminoisobutyric acid (Aib) residue [J].
Carpino, Louis A. ;
Abdel-Maksoud, Adel Ali ;
Mansour, E. M. E. ;
Zewail, Mohamed A. .
TETRAHEDRON LETTERS, 2007, 48 (41) :7404-7407
[9]   Emerging concepts in engineering extracellular matrix variants for directing cell phenotype [J].
Carson, Ashley E. ;
Barker, Thomas H. .
REGENERATIVE MEDICINE, 2009, 4 (04) :593-600
[10]   Anchorage of VEGF to the extracellular matrix conveys differential signaling responses to endothelial cells [J].
Chen, Tom T. ;
Luque, Alfonso ;
Lee, Sunyoung ;
Anderson, Sean M. ;
Segura, Tatiana ;
Iruela-Arispe, M. Luisa .
JOURNAL OF CELL BIOLOGY, 2010, 188 (04) :595-609