An optimised MALDI-TOF assay for phosphatidylcholine-specific phospholipase C.

Anal Methods

School of Chemical Sciences, The University of Auckland, Private Bag 92019, Victoria Street West, Auckland 1142, New Zealand. and Maurice Wilkins Centre for Molecular Biodiscovery, The University of Auckland, Private Bag 92019, Victoria Street West, Auckland 1142, New Zealand and Centre for Green Chemical Science, The University of Auckland, Private Bag 92019, Victoria Street West, Auckland 1142, New Zealand.

Published: February 2021

The Bacillus cereus phosphatidylcholine-specific phospholipase C (PC-PLCBc) is an enzyme that catalyses the hydrolysis of phosphatidylcholines into phosphocholine and 1,2-diacylglycerols. PC-PLCBc has found applications in both the food industry and in medicinal chemistry. Herein, we report our work in the development and optimisation of a matrix assisted laser desorption ionisation time-of-flight (MALDI-TOF) mass spectrometry-based assay to monitor PC-PLCBc activity. The use of one-phase and two-phase reaction systems to assess the inhibition of PC-PLCBc with different structural classes of inhibitors was compared. We also highlighted the advantage of our assay over the commonly used commercially available Amplex Red assay. This method will also be applicable to work on the activity and inhibition of other phospholipases.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d0ay02208jDOI Listing

Publication Analysis

Top Keywords

phosphatidylcholine-specific phospholipase
8
optimised maldi-tof
4
assay
4
maldi-tof assay
4
assay phosphatidylcholine-specific
4
phospholipase bacillus
4
bacillus cereus
4
cereus phosphatidylcholine-specific
4
pc-plcbc
4
phospholipase pc-plcbc
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!