Snake venom three-finger toxins and their potential in drug development targeting cardiovascular diseases

被引:30
|
作者
Kini, R. Manjunatha [1 ,2 ]
Koh, Cho Yeow [3 ]
机构
[1] Natl Univ Singapore, Fac Sci, Dept Biol Sci, Singapore 117558, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore 117600, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Med, Singapore 119228, Singapore
基金
英国医学研究理事会;
关键词
Venom; Three-finger toxins; Cardiovascular diseases; Structure; Drug development; PLATELET-AGGREGATION INHIBITOR; PROTEIN-COUPLED RECEPTORS; SHORT-NEUROTOXIN HOMOLOG; SENSING ION CHANNELS; BLACK MAMBA VENOM; PROLINE RESIDUES; ALPHA-2-BETA-1; INTEGRIN; 3-DIMENSIONAL STRUCTURE; HEMACHATUS-HAEMACHATUS; THROMBUS FORMATION;
D O I
10.1016/j.bcp.2020.114105
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cardiovascular diseases such as coronary and peripheral artery diseases, venous thrombosis, stroke, hypertension, and heart failure are enormous burden to health and economy globally. Snake venoms have been the sources of discovery of successful therapeutics targeting cardiovascular diseases. For example, the first-in-class angiotensin-converting enzyme inhibitor captopril was designed largely based on bradykinin-potentiating peptides from Bothrops jararaca venom. In the recent years, sensitive and high throughput approaches drive discovery and cataloging of new snake venom toxins. As one of the largest class of snake venom toxin, there are now > 700 sequences of three-finger toxins (3FTxs) available, many of which are yet to be studied. While the function of 3FTxs are normally associated with neurotoxicity, increasingly more 3FTxs have been characterized to have pharmacological effects on cardiovascular systems. Here we focus on this family of snake venom toxins and their potential in developing therapeutics against cardiovascular diseases.
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页数:10
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