Molecular basis of phospholipase A2 activity toward phospholipids with sn-1 substitutions

Research output: Contribution to journalJournal articleResearchpeer-review


We studied secretory phospholipase A(2) type IIA (sPLA(2)) activity toward phospholipids that are derivatized in the sn-1 position of the glycerol backbone. We explored what type of side group (small versus bulky groups, hydrophobic versus polar groups) can be introduced at the sn-1 position of the glycerol backbone of glycerophospholipids and at the same time be hydrolyzed by sPLA(2). The biophysical characterization revealed that the modified phospholipids can form multilamellar vesicles, and several of the synthesized sn-1 functionalized phospholipids were hydrolyzed by sPLA(2). Molecular dynamics simulations provided detailed insight on an atomic level that can explain the observed sPLA(2) activity toward the different phospholipid analogs. The simulations revealed that, depending on the nature of the side chain located at the sn-1 position, the group may interfere with an incoming water molecule that acts as the nucleophile in the enzymatic reaction. The simulation results are in agreement with the experimentally observed sPLA(2) activity toward the different phospholipid analogs.
Original languageEnglish
JournalBiophysical Journal
Issue number1
Pages (from-to)14-26
Number of pages13
Publication statusPublished - 2008

Fingerprint Dive into the research topics of 'Molecular basis of phospholipase A<sub>2</sub> activity toward phospholipids with <em>sn</em>-1 substitutions'. Together they form a unique fingerprint.

Cite this