A large scale high-throughput screen identifies chemical inhibitors of phosphatidylinositol 4-kinase type II alpha

0502931 - ÚOCHB 2020 RIV US eng J - Článek v odborném periodiku
Sengupta, N. - Jovic, M. - Barnaeva, E. - Kim, D. W. - Hu, X. - Southall, N. - Dejmek, Milan - Mejdrová, Ivana - Nencka, Radim - Bäumlová, Adriana - Chalupská, Dominika - Bouřa, Evžen - Ferrer, M. - Marugan, J. - Balla, T.
A large scale high-throughput screen identifies chemical inhibitors of phosphatidylinositol 4-kinase type II alpha.
Journal of Lipid Research. Roč. 60, č. 3 (2019), s. 683-693. ISSN 0022-2275. E-ISSN 1539-7262
Grant CEP: GA MŠMT(CZ) EF16_019/0000729
Institucionální podpora: RVO:61388963
Klíčová slova: phosphoinositide * endosome * vesicular traffic
Obor OECD: Biochemistry and molecular biology
Impakt faktor: 4.483, rok: 2019
Způsob publikování: Open access
https://www.jlr.org/content/60/3/683

The minor phospholipid, phosphatidylinositol 4-phosphate (PI4P), is emerging as a key regulator of lipid transfer in ER-membrane contact sites. Four different phosphatidylinositol 4-kinase (PI4K) enzymes generate PI4P in different membrane compartments supporting distinct cellular processes, many of which are crucial for the maintenance of cellular integrity but also hijacked by intracellular pathogens. While type III PI4Ks have been targeted by small molecular inhibitors, thus helping decipher their importance in cellular physiology, no inhibitors are available for the type II PI4Ks, which hinders investigations into their cellular functions. Here, we describe the identification of small molecular inhibitors of PI4K type II alpha (PI4K2A) by implementing a large scale small molecule high-throughput screening. A novel assay was developed that allows testing of selected inhibitors against PI4K2A in intact cells using a bioluminescence resonance energy transfer approach adapted to plate readers. The compounds disclosed here will pave the way to the optimization of PI4K2A inhibitors that can be used in cellular and animal studies to better understand the role of this enzyme in both normal and pathological states.
Trvalý link: http://hdl.handle.net/11104/0296502