Discovery and structure of a new inhibitor scaffold of the autophagy initiating kinase ULK1

• Published in: Bioorganic & medicinal chemistry Vol. 23; no. 17; pp. 5483 - 5488
• Main Authors: Lazarus, Michael B., Shokat, Kevan M.
• Format: Journal Article
• Language: English
• Published: OXFORD Elsevier Ltd 01.09.2015; Elsevier
• Subjects: Autophagy; Autophagy - genetics; Autophagy-Related Protein-1 Homolog; Biochemistry & Molecular Biology; Chemistry; Chemistry, Medicinal; Chemistry, Organic; Humans; Inhibitor; Intracellular Signaling Peptides and Proteins - genetics; Intracellular Signaling Peptides and Proteins - metabolism; Kinase; Life Sciences & Biomedicine; Molecular Structure; Pharmacology & Pharmacy; Physical Sciences; Protein-Serine-Threonine Kinases - genetics; Protein-Serine-Threonine Kinases - metabolism; Science & Technology; Structure; Inhibitor; Structure; Kinase; Autophagy; TARGET; CELLS; ACTIVATION; PHOSPHORYLATION; 3-PHOSPHOINOSITIDE-DEPENDENT KINASE-1; HOMOLOG; CANCER; YEAST; MOTION; ATG1 COMPLEX
• ISSN: 0968-0896; 1464-3391
• DOI: 10.1016/j.bmc.2015.07.034

[Display omitted] Energy homeostasis in eukaryotic cells is a complex and fundamental process that is misregulated in several human diseases. A key component of energy regulation is a process called autophagy that involves the recycling of cellular components. There has been much recent interest in studying the mechanism of autophagy to understand an important cellular process and to evaluate the therapeutic potential in targeting autophagy. Activation of a kinase called ULK1 initiates autophagy by driving downstream pathways that lead to the formation of double membrane bound vesicles that surround the cellular contents that are to be degraded. Here, we report the discovery of an inhibitor of ULK1 with improved selectivity and a high-resolution crystal structure of the compound bound to the kinase, which will be useful tools for studying autophagy in cells.