The Future of Peptide-based Drugs

被引:1551
作者
Craik, David J. [1 ]
Fairlie, David P. [1 ]
Liras, Spiros [2 ]
Price, David [2 ]
机构
[1] Univ Queensland, Div Chem & Struct Biol, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] Pfizer Inc, CVMED Med Chem, Worldwide Med Chem, Cambridge, MA 02139 USA
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
conformation; cyclic peptides; oral bioavailability; peptide scaffolds; screening; PROTEIN-COUPLED RECEPTORS; CALCIUM-CHANNEL BLOCKER; CYCLIC-PEPTIDES; N-METHYLATION; ORAL BIOAVAILABILITY; MOLECULAR SCAFFOLDS; MEDICINAL CHEMISTRY; INTEGRIN EXPRESSION; LIVING SUBJECTS; ALPHA-HELICES;
D O I
10.1111/cbdd.12055
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
The suite of currently used drugs can be divided into two categories traditional small molecule drugs with typical molecular weights of <500 Da but with oral bioavailability, and much larger biologics typically >5000 Da that are not orally bioavailable and need to be delivered via injection. Due to their small size, conventional small molecule drugs may suffer from reduced target selectivity that often ultimately manifests in human side-effects, whereas protein therapeutics tend to be exquisitely specific for their targets due to many more interactions with them, but this comes at a cost of low bioavailability, poor membrane permeability, and metabolic instability. The time has now come to reinvestigate new drug leads that fit between these two molecular weight extremes, with the goal of combining advantages of small molecules (cost, conformational restriction, membrane permeability, metabolic stability, oral bioavailability) with those of proteins (natural components, target specificity, high potency). This article uses selected examples of peptides to highlight the importance of peptide drugs, some potential new opportunities for their exploitation, and some difficult challenges ahead in this field.
引用
收藏
页码:136 / 147
页数:12
相关论文
共 79 条
[1]  
Adams DJ, 1999, DRUG DEVELOP RES, V46, P219
[2]   Chemical Re-engineering of Chlorotoxin Improves Bioconjugation Properties for Tumor Imaging and Targeted Therapy [J].
Akcan, Muharrem ;
Stroud, Mark R. ;
Hansen, Stacey J. ;
Clark, Richard J. ;
Daly, Norelle L. ;
Craik, David J. ;
Olson, James M. .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (03) :782-787
[3]   A ONE-VARIABLE TOPOGRAPHICAL DESCRIPTOR FOR THE BETA-TURNS OF PEPTIDES AND PROTEINS [J].
BALL, JB ;
ANDREWS, PR ;
ALEWOOD, PF ;
HUGHES, RA .
FEBS LETTERS, 1990, 273 (1-2) :15-18
[4]   Intestinal Permeability of Cyclic Peptides: Common Key Backbone Motifs Identified [J].
Beck, Johannes G. ;
Chatterjee, Jayanta ;
Laufer, Burkhardt ;
Kiran, Marelli Udaya ;
Frank, Andreas O. ;
Neubauer, Stefanie ;
Ovadia, Oded ;
Greenberg, Sarit ;
Gilon, Chaim ;
Hoffman, Amnon ;
Kessler, Horst .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (29) :12125-12133
[5]   Peptide drugs to target G protein-coupled receptors [J].
Bellmann-Sickert, Kathrin ;
Beck-Sickinger, Annette G. .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2010, 31 (09) :434-441
[6]   Improving oral bioavailability of peptides by multiple N-methylation: Somatostatin analogues [J].
Biron, Eric ;
Chatterjee, Jayanta ;
Ovadia, Oded ;
Langenegger, Daniel ;
Brueggen, Joseph ;
Hoyer, Daniel ;
Schmid, Herbert A. ;
Jelinek, Raz ;
Gilon, Chaim ;
Hoffman, Amnon ;
Kessler, Horst .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (14) :2595-2599
[7]  
Borel JF, 2002, WIEN KLIN WOCHENSCHR, V114, P433
[8]  
Bowersox S, 1997, DRUG METAB DISPOS, V25, P379
[9]   Assessing Helical Protein Interfaces for Inhibitor Design [J].
Bullock, Brooke N. ;
Jochim, Andrea L. ;
Arora, Paramjit S. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (36) :14220-14223
[10]   An alpha helix conformationally restricted peptide is recognized by cervical carcinoma patients' sera [J].
Calvo, JC ;
Choconta, KC ;
Diaz, D ;
Orozco, O ;
Bravo, MM ;
Espejo, F ;
Salazar, LM ;
Guzman, F ;
Patarroyo, ME .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (25) :5389-5394