Arrestin‐3‐Dependent Activation of c‐Jun N‐Terminal Kinases (JNKs)

Author:

Zhan Xuanzhi12,Kaoud Tamer S.3,Dalby Kevin N.3,Gurevich Eugenia V.1,Gurevich Vsevolod V.1

Affiliation:

1. Department of Pharmacology Vanderbilt University Nashville Tennessee

2. Current address: Tennessee Tech University Cookville Tennessee

3. Division of Chemical Biology & Medicinal Chemistry The University of Texas at Austin Austin Texas

Abstract

AbstractOnly 1 out of 4 mammalian arrestin subtypes, arrestin‐3, facilitates the activation of c‐Jun N‐terminal kinase (JNK) family kinases. Here, we describe two different sets of protocols used for elucidating the mechanisms involved. One is based on reconstitution of signaling modules from the following purified proteins: arrestin‐3, MKK4, MKK7, JNK1, JNK2, and JNK3. The main advantage of this method is that it unambiguously establishes which effects are direct because only intended purified proteins are present in these assays. The key drawback is that the upstream‐most kinases of these cascades, ASK1 or other MAP3Ks, are not available in purified form, limiting reconstitution to incomplete two‐kinase modules. The other approach is used for analyzing the effects of arrestin‐3 on JNK activation in intact cells. In this case, signaling modules include ASK1 and/or other MAP3Ks. However, as every cell expresses thousands of different proteins, their possible effects on the readout cannot be excluded. Nonetheless, the combination of in vitro reconstitution from purified proteins and cell‐based assays makes it possible to elucidate the mechanisms of arrestin‐3‐dependent activation of JNK family kinases. © 2023 Wiley Periodicals LLC.Basic Protocol 1: Construction of arrestin‐3‐scaffolded MKK4/7‐JNK1/2/3 signaling modules in vitro using purified proteinsAlternate Protocol 1: Characterization of arrestin‐3‐mediated JNK1/2 activation by MKK4/7 by measurement of JNK1/2 phosphorylation using immunoblotting with anti‐phospho‐JNK antibodySupport Protocol 1: Expression, purification, and activation of GST‐MKK4Support Protocol 2: Expression, purification, and activation of GST‐MKK7‐His6Support Protocol 3: Expression, purification, and activation of tagless JNK1Α1Support Protocol 4: Expression, purification, and activation of tagless JNK2Α2Basic Protocol 2: Analysis of the role of arrestin‐3 in ASK1/MKK4/MKK7‐induced JNK activation in intact cellsAlternate Protocol 2: Analysis of the role of arrestin‐3 in MKK4‐induced JNK activation in intact cellsBasic Protocol 3: Characterization of the biphasic effect of arrestin‐3 on ASK1/MKK7‐stimulated JNK phosphorylation in cells

Publisher

Wiley

Subject

Medical Laboratory Technology,Health Informatics,General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

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