CaM kinase phosphatase (CaMKP/PPM1F/POPX2) is specifically inactivated through gallate-mediated protein carbonylation

• Published in: Archives of biochemistry and biophysics 2022-05, Vol.720, p.109170-109170, Article 109170
• Main Authors: Akizuki, Kazutoshi, Ishikawa, Shun, Obatake, Rika, Ozaki, Hana, Shimoda, Nao, Nehira, Tatsuo, Yamazaki, Takeshi, Kinumi, Tomoya, Osawa, Jin, Sueyoshi, Noriyuki, Kameshita, Isamu, Shigeri, Yasushi, Ishida, Atsuhiko
• Format: Article
• Language: English
• Subjects: Calcium-Calmodulin-Dependent Protein Kinase Type 1 - chemistry; Chemical library; Covalent modification; Dephosphorylation; Oxidation-Reduction; Phosphoprotein Phosphatases - chemistry; Phosphorylation; Protein carbonyl; Protein Carbonylation; Protein Phosphatase 1 - genetics; Protein Phosphatase 1 - metabolism; Protein Phosphatase 2 - metabolism; Specific inhibition
• ISSN: 0003-9861; 1096-0384
• DOI: 10.1016/j.abb.2022.109170

CaMK phosphatase (CaMKP/PPM1F/POPX2) is a Mn2+-dependent, calyculin A/okadaic acid-insensitive Ser/Thr protein phosphatase that belongs to the PPM family. CaMKP is thought to be involved in regulation of not only various protein kinases, such as CaM kinases and p21-activated protein kinase, but also of cellular proteins regulated by phosphorylation. A large-scale screening of a chemical library identified gallic acid and some of its alkyl esters as novel CaMKP inhibitors highly specific to CaMKP. Surprisingly, they caused specific carbonylation of CaMKP, leading to its inactivation. Under the same conditions, no carbonylation nor inactivation was observed when PPM1A, which is affiliated with the same family as CaMKP, and λ-phosphatase were used. The carbonylation reaction was inhibited by SH compounds such as cysteamine in a dose-dependent manner with a concomitant decrease in CaMKP inhibition by ethyl gallate. The pyrogallol structure of gallate was necessary for the gallate-mediated carbonylation of CaMKP. Point mutations of CaMKP leading to impairment of phosphatase activity did not significantly affect the gallate-mediated carbonylation. Ethyl gallate resulted in almost complete inhibition of CaMKP under the conditions where the carbonylation level was nearly identical to that of CaMKP carbonylation via metal-catalyzed oxidation with ascorbic acid/FeSO4, which resulted in only a partial inhibition of CaMKP. The gallate-mediated carbonylation of CaMKP absolutely required divalent cations such as Mn2+, Cu2+, Co2+ and Fe2+, and was markedly enhanced by a phosphopeptide substrate. When MDA-MB-231 cells transiently expressing CaM kinase I, a CaMKP substrate, were treated by ethyl gallate, significant enhancement of phosphorylation of CaM kinase I was observed, suggesting that ethyl gallate can penetrate into cells to inactivate cellular CaMKP. All the presented data strongly support the hypothesis that CaMKP undergoes carbonylation of its specific amino acid residues by incubation with alkyl gallates and the divalent metal cations, leading to inactivation specific to CaMKP. •Gallic acid and some of its alkyl esters were identified as novel CaMKP inhibitors.•The inhibitors caused specific carbonylation of CaMKP, leading to its inactivation.•Neither carbonylation nor inactivation was observed when PPM1A or λPPase was used.•The gallate-mediated carbonylation required certain divalent metal cations.•The carbonylation was inhibited by SH compounds, and stimulate