Glutathione Transferase Photoaffinity Labeling Displays GST Induction by Safeners and Pathogen Infection

Author:

Font Farre Maria1,Brown Daniel2,König Maurice1,Killinger Brian J3,Kaschani Farnusch4,Kaiser Markus4,Wright Aaron T356,Burton Jonathan2,van der Hoorn Renier A L1

Affiliation:

1. The Plant Chemetics Laboratory, Department of Biology, University of Oxford , Oxford OX1 3RB, UK

2. Chemistry Research Laboratory, Department of Chemistry, University of Oxford , Oxford, Oxfordshire OX1 3TA, UK

3. Voiland School of Chemical Engineering and Bioengineering, Washington State University , Pullman, WA 99164, USA

4. ZMB Chemical Biology, Faculty of Biology, University of Duisburg-Essen , Essen 45141, Germany

5. Department of Biology, Baylor University , Waco, TX 76798, USA

6. Department of Chemistry & Biochemistry, Baylor University , Waco, TX 76706, USA

Abstract

Abstract Glutathione transferases (GSTs) represent a large and diverse enzyme family involved in the detoxification of small molecules by glutathione conjugation in crops, weeds and model plants. In this study, we introduce an easy and quick assay for photoaffinity labeling of GSTs to study GSTs globally in various plant species. The small-molecule probe contains glutathione, a photoreactive group and a minitag for coupling to reporter tags via click chemistry. Under UV irradiation, this probe quickly and robustly labels GSTs in crude protein extracts of different plant species. Purification and mass spectrometry (MS) analysis of labeled proteins from Arabidopsis identified 10 enriched GSTs from the Phi(F) and Tau(U) classes. Photoaffinity labeling of GSTs demonstrated GST induction in wheat seedlings upon treatment with safeners and in Arabidopsis leaves upon infection with avirulent bacteria. Treatment of Arabidopsis with salicylic acid (SA) analog benzothiadiazole (BTH) induces GST labeling independent of NPR1, the master regulator of SA. Six Phi- and Tau-class GSTs that are induced upon BTH treatment were identified, and their labeling was confirmed upon transient overexpression. These data demonstrate that GST photoaffinity labeling is a useful approach to studying GST induction in crude extracts of different plant species upon different types of stress.

Funder

BBSRC

Biotechnology and Biological Sciences Research Council

FP7 Ideas: European Research Council

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science,Physiology,General Medicine

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