New approaches for cell-specific targeting: identification of cell-selective peptides from combinatorial libraries

被引:91
作者
Brown, KC [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Internal Med, Ctr Biomed Intervent, Dallas, TX 75390 USA
关键词
D O I
10.1016/S1367-5931(99)00045-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Peptides that recognize specific cell types promise to be valuable tools both in research and clinical applications. Cell-specific peptides can be useful as drug delivery vehicles, diagnostic agents, affinity reagents for cell purification, gene therapy delivery agents, and research tools to probe the nature of a cell's surface. Recently, cell-specific targeting-peptides have been identified by phage-display selections against purified cell-surface markers, whole cells in tissue culture, and even tissues within live animals. These methods for identifying cell-targeting peptides will certainly increase the tools available to the scientist for cell-specific targeting.
引用
收藏
页码:16 / 21
页数:6
相关论文
共 38 条
[1]
Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model [J].
Arap, W ;
Pasqualini, R ;
Ruoslahti, E .
SCIENCE, 1998, 279 (5349) :377-380
[2]
Semirational design of a potent, artificial agonist of fibroblast growth factor receptors [J].
Ballinger, MD ;
Shyamala, V ;
Forrest, LD ;
Deuter-Reinhard, M ;
Doyle, LV ;
Wang, JX ;
Panganiban-Lustan, L ;
Stratton, JR ;
Apell, G ;
Winter, JA ;
Doyle, MV ;
Rosenberg, S ;
Kavanaugh, WM .
NATURE BIOTECHNOLOGY, 1999, 17 (12) :1199-1204
[3]
Toward cell-targeting gene therapy vectors: Selection of cell-binding peptides from random peptide-presenting phage libraries [J].
Barry, MA ;
Dower, WJ ;
Johnston, SA .
NATURE MEDICINE, 1996, 2 (03) :299-305
[4]
DNA-based selection and screening of peptide ligands [J].
Bartoli, F ;
Nuzzo, M ;
Urbanelli, L ;
Bellintani, F ;
Prezzi, C ;
Cortese, R ;
Monaci, P .
NATURE BIOTECHNOLOGY, 1998, 16 (11) :1068-1073
[5]
Burg MA, 1999, CANCER RES, V59, P2869
[6]
An adenovirus vector with genetically modified fibers demonstrates expanded tropism via utilization of a coxsackievirus and adenovirus receptor-independent cell entry mechanism [J].
Dmitriev, I ;
Krasnykh, V ;
Miller, CR ;
Wang, MH ;
Kashentseva, E ;
Mikheeva, G ;
Belousova, N ;
Curiel, DT .
JOURNAL OF VIROLOGY, 1998, 72 (12) :9706-9713
[7]
ISOLATION OF A PEPTIDE ANTAGONIST TO THE THROMBIN RECEPTOR USING PHAGE DISPLAY [J].
DOORBAR, J ;
WINTER, G .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 244 (04) :361-369
[8]
Anti-cancer activity of targeted pro-apoptotic peptides [J].
Ellerby, HM ;
Arap, W ;
Ellerby, LM ;
Kain, R ;
Andrusiak, R ;
Del Rio, G ;
Krajewski, S ;
Lombardo, CR ;
Rao, R ;
Ruoslahti, E ;
Bredesen, DE ;
Pasqualini, R .
NATURE MEDICINE, 1999, 5 (09) :1032-1038
[9]
The development of monoclonal antibodies for the therapy of cancer [J].
Farah, RA ;
Clinchy, B ;
Herrera, L ;
Vitetta, ES .
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 1998, 8 (3-4) :321-356
[10]
Selection of a histidine-containing inhibitor of gelatinases through deconvolution of combinatorial tetrapeptide libraries [J].
Ferry, G ;
Boutin, JA ;
Atassi, G ;
Fauchere, JL ;
Tucker, GC .
MOLECULAR DIVERSITY, 1997, 2 (03) :135-146