Abstract

A simple, accurate, sensitive and robust assay that can rapidly and specifically measure the death of target cells would have applications in many areas of biomedicine and particularly for the development of novel cellular- and immune-therapeutics. In this study, we describe a novel cytotoxicity assay, termed the Matador assay, which takes advantage of the extreme brightness, stability and glow-like characteristics of recently discovered novel marine luciferases and their engineered derivatives. The assay involves expression of a luciferase of interest in target cells in a manner so that it is preferentially retained within the healthy cells but is either released from dead and dying cells or whose activity can be preferentially measured in dead and dying cells. We demonstrate that this assay is highly sensitive, specific, rapid, and can be performed in a single-step manner without the need for any expensive equipment. We further validate this assay by demonstrating its ability to detect cytotoxicity induced by several cellular and immune-therapeutic agents including antibodies, natural killer cells, chimeric antigen receptor expressing T cells and a bispecific T cell engager.

Details

Title
Development and characterization of a novel luciferase based cytotoxicity assay
Author
Matta, Hittu 1 ; Gopalakrishnan, Ramakrishnan 1   VIAFID ORCID Logo  ; Choi, Sunju 1 ; Prakash, Rekha 1 ; Natarajan, Venkatesh 1 ; Prins, Ruben 1 ; Gong, Songjie 1 ; Chitnis, Saurabh D 1 ; Kahn, Michael 1   VIAFID ORCID Logo  ; Xu, Han 1 ; Chaudhary, Vishan 1 ; Soni, Adam 1 ; Sernas, Jennifer 1 ; Khan, Prottasha 1 ; Wang, Dan 1 ; Chaudhary, Preet M 1 

 Jane Anne Nohl Division of Hematology and Center for the Study of Blood Diseases, University of Southern California, Keck School of Medicine, Los Angeles, California, United States of America 
First page
1
Publication year
2018
Publication date
Jan 2018
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1993418932
Copyright
© 2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.