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Crystal structure of phospholipase A 2 in complex with 1‐naphthaleneacetic acid
Author(s) -
Dileep Kalarickal V.,
Remya Chandran,
Tintu Ignatius,
Mandal Pradeep K.,
Karthe Ponnuraj,
Haridas Madathilkovilakathu,
Sadasivan Chittalakkottu
Publication year - 2018
Publication title -
iubmb life
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.132
H-Index - 113
eISSN - 1521-6551
pISSN - 1521-6543
DOI - 10.1002/iub.1924
Subject(s) - isothermal titration calorimetry , phospholipase a2 , chemistry , active site , stereochemistry , enzyme , arachidonic acid , phospholipase a , substrate (aquarium) , biochemistry , biology , ecology
Phospholipase A 2 (PLA 2 ) is one of the rate limiting enzymes involved in the production of arachidonic acid, a potent inflammatory mediator. PLA 2 is widely distributed all over the animal kingdom. It is also seen in inflammatory exudation and venoms of different organisms. The studies demonstrated that PLA 2 inhibitors have broad spectrum activities that they can either be used against inflammation or envenomation. In this study, the inhibitory activity of 1‐napthaleneacetic acid (NAA) against porcine pancreatic PLA 2 has been explained through isothermal titration calorimetry and enzyme kinetics studies. The atomic level of interactions of NAA with PLA 2 was also studied using X‐ray crystallography. Apart from these findings, the theoretical binding affinities and mode of interactions of two naphthalene‐based NSAIDs such as naproxen (NAP) and nabumetone (NAB) were studied through molecular modeling. The studies proved that the selected ligands are binding at the doorway of the active site cleft and hindering the substrate entry to the active site. The study brings out a potential scaffold for the designing of broad spectrum PLA 2 inhibitors which can be used for inflammation or envenomation. © 2018 IUBMB Life, 70(10):995–1001, 2018