Positive surface charge inhibition of phospholipase A2 in mixed monolayer systems

Cheryl Willman, H. Stewart Hendrickson

Research output: Contribution to journalArticlepeer-review

Abstract

Inhibition of pancreatic phospholipase A2 by surface-active local anesthetics was recently reported by this laboratory to be due to enzyme-anesthetic interaction in the subphase and surface effects. In order to study surface effects in the absence of subphase effects, a long-chain tetracaine analog which was completely insoluble in the subphase, dimethylaminoethyl p-decoxybenzoate, was synthesized. To determine if inhibition was due to the positive surface charge of the analog or some other effect related to structure, the analog's inhibitory effects were compared with those of octadecylamine. Analog-didecanoyl lecithin (PC) monolayers showed nonideal mixing as evidenced by a condensing effect, while octadecylamine-didecanoyl PC monolayers showed ideal mixing. The apparent pK′a of octadecylamine-dioctanoyl PC micelles (1:4) was 9.9, while that of the analog-dioctanoyl PC micelles (1:4) was 7.6. At pH values where both amines were fully protonated, inhibition of both porcine pancreatic and Crotalus adamanteus phospholipase A2 on the mixed films was maximal and similar (94-97%). Inhibition decreased with increasing pH and decreasing surface charge on both mixed films and at pH values where both amines were 50% protonated, inhibition was half-maximal. At pH 8.5, where the analog was unprotonated, no inhibition was observed. Thus, inhibition of phospholipase A2 appears to be due to a positive surface charge alone rather than any effects related to anesthetic structure or spacing in the monolayer.

Original languageEnglish (US)
Pages (from-to)298-305
Number of pages8
JournalArchives of Biochemistry and Biophysics
Volume191
Issue number1
DOIs
StatePublished - Nov 1978

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology

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