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Updated: May 6, 2026

Kinase Inhibitor Screening In Self-assembled Human Protein Microarrays
Published on: October 23, 2019
Screening of protein kinase inhibitors and knockdown experiments identified four kinases that affect mitochondrial
Kanako Sugawara1, Makoto Fujikawa, Masasuke Yoshida
1International Cooperative Research Project (ICORP), ATP Synthesis Regulation Project, Japan Science and Technology Agency, Aomi 2-3-6, Tokyo 135-0064, Japan; Department of Molecular Bioscience, Kyoto Sangyo University, Kamigamo-Motoyama, Kyoto 603-8555, Japan.
Abstract:
Mitochondrial ATP synthase, a major ATP supplier in respiring cells, should be regulated in amount and in activity to respond to the varying demands of cells for ATP. We screened 80 protein kinase inhibitors and found that HeLa cells treated with four inhibitors exhibited reduced mitochondrial ATP synthesis activity. Consistently, knockdown of their target kinases (PKA, PKCδ, CaMKII and smMLCK) resulted in a decrease in mitochondrial ATP synthesis activity. Among them, mitochondria of smMLCK-knockdown cells contained only a small amount of ATP synthase, while the α- and β-subunits of ATP synthase were produced normally, suggesting that smMLCK affects assembly (or decay) of ATP synthase.
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