Discovery of the novel autophagy inhibitor aumitin that targets mitochondrial complex I
Macroautophagy is a conserved eukaryotic process for degradation of cellular components in response to lack of nutrients. It is involved in the development of diseases, notably cancer and neurological disorders including Parkinson's disease. Small molecule autophagy modulators have proven to be...
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Veröffentlicht in: | Chemical science (Cambridge) 2018-03, Vol.9 (11), p.314-322 |
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creator | Robke, Lucas Futamura, Yushi Konstantinidis, Georgios Wilke, Julian Aono, Harumi Mahmoud, Zhwan Watanabe, Nobumoto Wu, Yao-Wen Osada, Hiroyuki Laraia, Luca Waldmann, Herbert |
description | Macroautophagy is a conserved eukaryotic process for degradation of cellular components in response to lack of nutrients. It is involved in the development of diseases, notably cancer and neurological disorders including Parkinson's disease. Small molecule autophagy modulators have proven to be valuable tools to dissect and interrogate this crucial metabolic pathway and are in high demand. Phenotypic screening for autophagy inhibitors led to the discovery of the novel autophagy inhibitor aumitin. Target identification and confirmation revealed that aumitin inhibits mitochondrial respiration by targeting complex I. We show that inhibition of autophagy by impairment of mitochondrial respiration is general for several mitochondrial inhibitors that target different mitochondrial complexes. Our findings highlight the importance of mitochondrial respiration for autophagy regulation.
Phenotypic screening for autophagy inhibitors followed by target identification resulted in the discovery of aumitin, a new autophagy inhibitor that inhibits mitochondrial respiration by targeting complex I. |
doi_str_mv | 10.1039/c7sc05040b |
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Phenotypic screening for autophagy inhibitors followed by target identification resulted in the discovery of aumitin, a new autophagy inhibitor that inhibits mitochondrial respiration by targeting complex I.</description><identifier>ISSN: 2041-6520</identifier><identifier>ISSN: 2041-6539</identifier><identifier>EISSN: 2041-6539</identifier><identifier>DOI: 10.1039/c7sc05040b</identifier><identifier>PMID: 29732085</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Autophagy ; Chemistry ; Inhibitors ; Modulators ; Nutrients ; Parkinson's disease ; Respiration ; Target recognition</subject><ispartof>Chemical science (Cambridge), 2018-03, Vol.9 (11), p.314-322</ispartof><rights>Copyright Royal Society of Chemistry 2018</rights><rights>This journal is © The Royal Society of Chemistry 2018 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-f084c99afbafb4ec2609107ad87cf11644408910efc7f23a7f1b78cd04f20bc73</citedby><cites>FETCH-LOGICAL-c507t-f084c99afbafb4ec2609107ad87cf11644408910efc7f23a7f1b78cd04f20bc73</cites><orcidid>0000-0001-6692-3412 ; 0000-0002-9606-7247 ; 0000-0002-2573-8736</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916016/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916016/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,550,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29732085$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-158854$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Robke, Lucas</creatorcontrib><creatorcontrib>Futamura, Yushi</creatorcontrib><creatorcontrib>Konstantinidis, Georgios</creatorcontrib><creatorcontrib>Wilke, Julian</creatorcontrib><creatorcontrib>Aono, Harumi</creatorcontrib><creatorcontrib>Mahmoud, Zhwan</creatorcontrib><creatorcontrib>Watanabe, Nobumoto</creatorcontrib><creatorcontrib>Wu, Yao-Wen</creatorcontrib><creatorcontrib>Osada, Hiroyuki</creatorcontrib><creatorcontrib>Laraia, Luca</creatorcontrib><creatorcontrib>Waldmann, Herbert</creatorcontrib><title>Discovery of the novel autophagy inhibitor aumitin that targets mitochondrial complex I</title><title>Chemical science (Cambridge)</title><addtitle>Chem Sci</addtitle><description>Macroautophagy is a conserved eukaryotic process for degradation of cellular components in response to lack of nutrients. It is involved in the development of diseases, notably cancer and neurological disorders including Parkinson's disease. Small molecule autophagy modulators have proven to be valuable tools to dissect and interrogate this crucial metabolic pathway and are in high demand. Phenotypic screening for autophagy inhibitors led to the discovery of the novel autophagy inhibitor aumitin. Target identification and confirmation revealed that aumitin inhibits mitochondrial respiration by targeting complex I. We show that inhibition of autophagy by impairment of mitochondrial respiration is general for several mitochondrial inhibitors that target different mitochondrial complexes. Our findings highlight the importance of mitochondrial respiration for autophagy regulation.
Phenotypic screening for autophagy inhibitors followed by target identification resulted in the discovery of aumitin, a new autophagy inhibitor that inhibits mitochondrial respiration by targeting complex I.</description><subject>Autophagy</subject><subject>Chemistry</subject><subject>Inhibitors</subject><subject>Modulators</subject><subject>Nutrients</subject><subject>Parkinson's disease</subject><subject>Respiration</subject><subject>Target recognition</subject><issn>2041-6520</issn><issn>2041-6539</issn><issn>2041-6539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>D8T</sourceid><recordid>eNpdkstv1DAQxiMEolXphTvIEheEFBi_4uSCVLY8KlXiwOtoOV574yqJt7ZT2P-egS0LxbJk-5vfjEbzuaoeU3hJgXevrMoWJAjo71XHDAStG8m7-4c7g6PqNOcrwMU5lUw9rI5YpziDVh5X385DtvHGpR2JnpTBkRlfIzFLidvBbHYkzEPoQ4kJtSmUMCNlCikmbVzJBKVohzivUzAjsXHaju4HuXhUPfBmzO709jypvrx7-3n1ob78-P5idXZZWwmq1B5aYbvO-B63cJY10FFQZt0q6ylthBDQouK8VZ5xozztVWvXIDyD3ip-UtX7uvm72y693qYwmbTT0QR9Hr6e6Zg2epkWTWXbSoH86z2P8OTW1s0lmfFO2t3IHAa9iTdadrQB2mCB57cFUrxeXC56wgm6cTSzi0vWDLhU0LSUIfrsP_QqLmnGcSBFBXA0pEPqxZ6yKeacnD80Q0H_sliv1KfVb4vfIPz03_YP6B9DEXiyB1K2h-jfP8J_AvSDrI8</recordid><startdate>20180321</startdate><enddate>20180321</enddate><creator>Robke, Lucas</creator><creator>Futamura, Yushi</creator><creator>Konstantinidis, Georgios</creator><creator>Wilke, Julian</creator><creator>Aono, Harumi</creator><creator>Mahmoud, Zhwan</creator><creator>Watanabe, Nobumoto</creator><creator>Wu, Yao-Wen</creator><creator>Osada, Hiroyuki</creator><creator>Laraia, Luca</creator><creator>Waldmann, Herbert</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><scope>ADHXS</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>D93</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0001-6692-3412</orcidid><orcidid>https://orcid.org/0000-0002-9606-7247</orcidid><orcidid>https://orcid.org/0000-0002-2573-8736</orcidid></search><sort><creationdate>20180321</creationdate><title>Discovery of the novel autophagy inhibitor aumitin that targets mitochondrial complex I</title><author>Robke, Lucas ; Futamura, Yushi ; Konstantinidis, Georgios ; Wilke, Julian ; Aono, Harumi ; Mahmoud, Zhwan ; Watanabe, Nobumoto ; Wu, Yao-Wen ; Osada, Hiroyuki ; Laraia, Luca ; Waldmann, Herbert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-f084c99afbafb4ec2609107ad87cf11644408910efc7f23a7f1b78cd04f20bc73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Autophagy</topic><topic>Chemistry</topic><topic>Inhibitors</topic><topic>Modulators</topic><topic>Nutrients</topic><topic>Parkinson's disease</topic><topic>Respiration</topic><topic>Target recognition</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Robke, Lucas</creatorcontrib><creatorcontrib>Futamura, Yushi</creatorcontrib><creatorcontrib>Konstantinidis, Georgios</creatorcontrib><creatorcontrib>Wilke, Julian</creatorcontrib><creatorcontrib>Aono, Harumi</creatorcontrib><creatorcontrib>Mahmoud, Zhwan</creatorcontrib><creatorcontrib>Watanabe, Nobumoto</creatorcontrib><creatorcontrib>Wu, Yao-Wen</creatorcontrib><creatorcontrib>Osada, Hiroyuki</creatorcontrib><creatorcontrib>Laraia, Luca</creatorcontrib><creatorcontrib>Waldmann, Herbert</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Umeå universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Umeå universitet</collection><collection>SwePub Articles full text</collection><jtitle>Chemical science (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Robke, Lucas</au><au>Futamura, Yushi</au><au>Konstantinidis, Georgios</au><au>Wilke, Julian</au><au>Aono, Harumi</au><au>Mahmoud, Zhwan</au><au>Watanabe, Nobumoto</au><au>Wu, Yao-Wen</au><au>Osada, Hiroyuki</au><au>Laraia, Luca</au><au>Waldmann, Herbert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Discovery of the novel autophagy inhibitor aumitin that targets mitochondrial complex I</atitle><jtitle>Chemical science (Cambridge)</jtitle><addtitle>Chem Sci</addtitle><date>2018-03-21</date><risdate>2018</risdate><volume>9</volume><issue>11</issue><spage>314</spage><epage>322</epage><pages>314-322</pages><issn>2041-6520</issn><issn>2041-6539</issn><eissn>2041-6539</eissn><abstract>Macroautophagy is a conserved eukaryotic process for degradation of cellular components in response to lack of nutrients. 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subjects | Autophagy Chemistry Inhibitors Modulators Nutrients Parkinson's disease Respiration Target recognition |
title | Discovery of the novel autophagy inhibitor aumitin that targets mitochondrial complex I |
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