TY - JOUR
T1 - Therapeutic peptides
T2 - Targeting the mitochondrion to modulate apoptosis
AU - Jacotot, Etienne
AU - Deniaud, Aurélien
AU - Borgne-Sanchez, Annie
AU - Touat, Zahia
AU - Briand, Jean Paul
AU - Le Bras, Morgane
AU - Brenner, Catherine
N1 - Funding Information:
This work is supported by grants from l'Association pour la Recherche sur le Cancer (ARC), la Fondation pour la Recherche Médicale (FRM), the Ministère délégué à la Recherche et aux Nouvelles Technologies (MRNT) to C.B. (GenHomme Programs No. 01H0480 and No. 03L297) and E.J. (GenHomme Programs No. 01H0476 and N°03L292), Agence Nationale pour la Valorisation de la Recherche (ANVAR) to E.J. (No. R0209333Q and No. A0404096Q) and CB (no. A0505001). AD and MLB received fellowships from MRNT and from the CNRS, respectively.
PY - 2006/9/1
Y1 - 2006/9/1
N2 - 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.
AB - 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.
KW - Apoptosis
KW - Bcl-2
KW - Mitochondrion
KW - Peptides
KW - Permeability transition
UR - http://www.scopus.com/inward/record.url?scp=33748953187&partnerID=8YFLogxK
U2 - 10.1016/j.bbabio.2006.07.002
DO - 10.1016/j.bbabio.2006.07.002
M3 - Review article
C2 - 16928356
AN - SCOPUS:33748953187
SN - 0005-2728
VL - 1757
SP - 1312
EP - 1323
JO - Biochimica et Biophysica Acta - Bioenergetics
JF - Biochimica et Biophysica Acta - Bioenergetics
IS - 9-10
ER -