Measuring Phospholipase D Enzymatic Activity Through Biochemical and Imaging Methods. Academic Article uri icon

Overview

abstract

  • The phospholipase D (PLD) enzymatic superfamily regulates a wide range of cell biological and physiological pathways, including platelet activation, immune responses, cancer, and spermatogenesis. The three main enzymatic actions of the superfamily entail (i) hydrolyzing membrane phospholipids (phosphatidylcholine (PC) and cardiolipin) to generate choline and the second messenger signaling lipid phosphatidic acid (PA), (ii) using ethanol to transphosphatidylate PC to generate the long-lived metabolite phosphatidylethanol, and (iii) hydrolyzing RNA transcripts to generate piRNAs, the third form of endogenous RNAi. We discuss briefly previously published methods for in vitro and in vivo detection and imaging of PA, and focus on production, purification, and in vitro endonuclease activity analysis for human PLD6, a mitochondrial-tethered isoform with roles in fertility, cancer, and neuronal homeostasis.

publication date

  • October 22, 2016

Research

keywords

  • Enzyme Assays
  • Mitochondrial Proteins
  • Molecular Imaging
  • Phospholipase D
  • RNA, Messenger

Identity

PubMed Central ID

  • PMC5708542

Scopus Document Identifier

  • 85001608946

Digital Object Identifier (DOI)

  • 10.1016/bs.mie.2016.09.041

PubMed ID

  • 28063496

Additional Document Info

volume

  • 583