Proteases as therapeutics

被引:149
作者
Craik, Charles S. [1 ]
Page, Michael J. [1 ]
Madison, Edwin L. [2 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94131 USA
[2] Catalyst Biosci, San Francisco, CA 94080 USA
关键词
procoagulant; protease therapy; protein degradation; protein engineering; trypsin fold; ACTIVATED PROTEIN-C; TISSUE-PLASMINOGEN-ACTIVATOR; RECOMBINANT-FACTOR-VIIA; ACUTE MYOCARDIAL-INFARCTION; FRONT-LOADED ALTEPLASE; CRYSTAL-STRUCTURE; COAGULATION-FACTOR; ALBUMIN FUSION; SEVERE SEPSIS; FACTOR-IX;
D O I
10.1042/BJ20100965
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
Proteases are an expanding class of drugs that hold great promise. The U.S. FDA (Food and Drug Administration) has approved 12 protease therapies, and a number of next generation or completely new proteases are in clinical development. Although they are a well-recognized class of targets for inhibitors, proteases themselves have not typically been considered as a drug class despite their application in the clinic over the last several decades; initially as plasma fractions and later as purified products. Although the predominant use of proteases has been in treating cardiovascular disease, they are also emerging as useful agents in the treatment of sepsis, digestive disorders, inflammation, cystic fibrosis, retinal disorders, psoriasis and other diseases. In the present review, we outline the history of proteases as therapeutics, provide an overview of their current clinical application, and describe several approaches to improve and expand their clinical application. Undoubtedly, our ability to harness proteolysis for disease treatment will increase with our understanding of protease biology and the molecular mechanisms responsible. New technologies for rationally engineering proteases, as well as improved delivery options, will expand greatly the potential applications of these enzymes. The recognition that proteases are, in fact, an established class of safe and efficacious drugs will stimulate investigation of additional therapeutic applications for these enzymes. Proteases therefore have a bright future as a distinct therapeutic class with diverse clinical applications.
引用
收藏
页码:1 / 16
页数:16
相关论文
共 191 条
[71]   Recovery from botulinum neurotoxin poisoning in vivo [J].
Keller, JE .
NEUROSCIENCE, 2006, 139 (02) :629-637
[72]   Crystal structure of active site-inhibited human coagulation factor VIIa (des-Gla) [J].
Kemball-Cook, G ;
Johnson, DJD ;
Tuddenham, EGD ;
Harlos, K .
JOURNAL OF STRUCTURAL BIOLOGY, 1999, 127 (03) :213-223
[73]   A new approach to treatment of bleeding episodes in young hemophilia patients:: a single bolus megadose of recombinant activated factor VII (NovoSeven®) [J].
Kenet, G ;
Lubetsky, A ;
Luboshitz, J ;
Martinowitz, U .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (03) :450-455
[74]  
Keyt Bruce A., 1996, P435
[76]   A review on the nonoperative removal of necrotic tissue from burn wounds [J].
Klasen, HJ .
BURNS, 2000, 26 (03) :207-222
[77]   Molecular diversity of anticoagulants from haematophagous animals [J].
Koh, Cho Yeow ;
Kini, R. Manjunatha .
THROMBOSIS AND HAEMOSTASIS, 2009, 102 (03) :437-453
[78]  
Komata T, 2001, CANCER RES, V61, P5796
[79]   Streptokinase - the drug of choice for thrombolytic therapy [J].
Kunamneni, Adinarayana ;
Abdelghani, Thaer Taleb Abed ;
Ellaiah, Poluri .
JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 2007, 23 (01) :9-23
[80]   ISOLATION AND CHARACTERIZATION OF A CDNA CODING FOR HUMAN FACTOR-IX [J].
KURACHI, K ;
DAVIE, EW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (21) :6461-6464