Identification of Lys49-PLA2 from crude venom of Crotalus atrox as a human neutrophil-calcium modulating protein.
10.4196/kjpp.2016.20.2.177
- Author:
Md. Tipu SULTAN
1
;
Hong Mei LI
;
Yong Zu LEE
;
Soon Sung LIM
;
Dong Keun SONG
Author Information
1. Department of Pharmacology, Institute of Natural Medicine, College of Medicine, Hallym University, Chuncheon 24252, Korea. limss@hallym.ac.kr dksong@hallym.ac.kr
- Publication Type:Original Article
- Keywords:
Crotalus atrox;
Human neutrophils;
Intracellular free-calcium concentration;
Lys49-PLA2;
Phosphodiesterase I
- MeSH:
Calcium Channels;
Chromatography, High Pressure Liquid;
Crotalus*;
Electrophoresis, Polyacrylamide Gel;
Humans*;
Membranes;
Neutrophils;
Phosphodiesterase I;
Phospholipases A2;
S Phase;
Venoms*
- From:The Korean Journal of Physiology and Pharmacology
2016;20(2):177-183
- CountryRepublic of Korea
- Language:English
-
Abstract:
We fortuitously observed a human neutrophil intracellular free-calcium concentration ([Ca2+]i) increasing activity in the commercially available phosphodiesterase I (PDE I), which is actually dried crude venom of Crotalus atrox. As this activity was not observed with another commercially available pure PDE I, we tried to find out the causative molecule(s) present in 'crude' PDE, and identified Lys49-phospholipase A2 (Lys49-PLA2 or K49-PLA2), a catalytically inactive protein which belongs to the phospholipase A2 family, by activity-driven three HPLC (reverse phase, size exclusion, reverse phase) steps followed by SDS-PAGE and LC-MS/MS. K49-PLA2 induced Ca2+ infl ux in human neutrophils without any cytotoxic eff ect. Two calcium channel inhibitors, 2-aminoetoxydiphenyl borate (2-APB) (30 microM) and SKF-96365 (20 microM) signifi cantly inhibited K49-PLA2-induced [Ca2+]i increase. These results suggest that K49-PLA2 modulates [Ca2+]i in human neutrophils via 2-APB- and SKF-96365-sensitive calcium channels without causing membrane disruption.
