Human pannexin 1 channel is not phosphorylated by Src tyrosine kinase at Tyr199 and Tyr309

Author:

Ruan Zheng1ORCID,Lee Junuk1ORCID,Li Yangyang1,Du Juan1ORCID,Lü Wei1ORCID

Affiliation:

1. Department of Structural Biology, Van Andel Institute

Abstract

Protein phosphorylation is one of the major molecular mechanisms regulating protein activity and function throughout the cell. Pannexin 1 (PANX1) is a large-pore channel permeable to ATP and other cellular metabolites. Its tyrosine phosphorylation and subsequent activation have been found to play critical roles in diverse cellular conditions, including neuronal cell death, acute inflammation, and smooth muscle contraction. Specifically, the non-receptor kinase Src has been reported to phosphorylate Tyr198 and Tyr308 of mouse PANX1 (equivalent to Tyr199 and Tyr309 of human PANX1), resulting in channel opening and ATP release. Although the Src-dependent PANX1 activation mechanism has been widely discussed in the literature, independent validation of the tyrosine phosphorylation of PANX1 has been lacking. Here, we show that commercially available antibodies against the two phosphorylation sites mentioned above—which were used to identify endogenous PANX1 phosphorylation at these two sites—are nonspecific and should not be used to interpret results related to PANX1 phosphorylation. We further provide evidence that neither tyrosine residue is a major phosphorylation site for Src kinase in heterologous expression systems. We call on the field to re-examine the existing paradigm of tyrosine phosphorylation-dependent activation of the PANX1 channel.

Funder

American Heart Association

National Institute of Neurological Disorders and Stroke

National Institute of General Medical Sciences

McKnight Endowment Fund for Neuroscience

Esther A. and Joseph Klingenstein Fund

Pew Charitable Trusts

Alfred P. Sloan Foundation

Publisher

eLife Sciences Publications, Ltd

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