Therapeutic peptides: Targeting the mitochondrion to modulate apoptosis

被引:24
|
作者
Jacotot, Etienne
Deniaud, Aurelien
Borgne-Sanchez, Annie
Touat, Zahia
Briand, Jean-Paul
Le Bras, Morgane
Brenner, Catherine
机构
[1] Univ Versailles, CNRS, UMR 8159, F-78035 Versailles, France
[2] Theraptosis SA, Theraptosis Res Lab, F-75015 Paris, France
[3] CNRS, UPR 9021, F-67084 Strasbourg, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2006年 / 1757卷 / 9-10期
关键词
peptides; mitochondrion; permeability transition; apoptosis; Bcl-2; PERMEABILITY TRANSITION PORE; ADENINE-NUCLEOTIDE TRANSLOCATOR; BCL-2 FAMILY PROTEINS; CYTOCHROME-C RELEASE; CHEMOTHERAPY-INDUCED APOPTOSIS; DEPENDENT ANION CHANNEL; CELL-DEATH; MEMBRANE PERMEABILIZATION; CYCLOPHILIN-D; PHARMACOLOGICAL MANIPULATION;
D O I
10.1016/j.bbabio.2006.07.002
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
For many years, medical drug discovery has extensively exploited peptides as lead compounds. Currently, novel structures of therapeutic peptides are derived from active pre-existing peptides or from high-throughput screening, and optimized following a rational drug design approach. Molecules of interest may prove their ability to influence the disease outcome in animal models and must respond to a set of criteria based on toxicity studies, ease of administration, the cost of their synthesis, and logistic for clinical use to validate it as a good candidate in a therapeutic perspective. This applies to the potential use of peptides to target one central intracellular organelle, the mitochondrion, to modulate (i.e. activate or prevent) apoptosis. Putative mitochondrial protein targets and the strategies already elaborated to correct the defects linked to these proteins (overexpression, inactivation, mutation..., etc.) are described, and recent advances that led or may lead to the conception of therapeutic peptides via a specific action on these mitochondrial targets in the future are discussed. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1312 / 1323
页数:12
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