Catechol-containing compounds are a broad class of protein aggregation inhibitors: Redox state is a key determinant of the inhibitory activities
A range of neurodegenerative and related aging diseases, such as Alzheimer’s disease and type 2 diabetes, are linked to toxic protein aggregation. Yet the mechanisms of protein aggregation inhibition by small molecule inhibitors remain poorly understood, in part because most protein targets of aggre...
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Veröffentlicht in: | Pharmacological research 2022-10, Vol.184, p.106409-106409, Article 106409 |
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creator | Velander, Paul Wu, Ling Hildreth, Sherry B. Vogelaar, Nancy J. Mukhopadhyay, Biswarup Helm, Richard F. Zhang, Shijun Xu, Bin |
description | A range of neurodegenerative and related aging diseases, such as Alzheimer’s disease and type 2 diabetes, are linked to toxic protein aggregation. Yet the mechanisms of protein aggregation inhibition by small molecule inhibitors remain poorly understood, in part because most protein targets of aggregation assembly are partially unfolded or intrinsically disordered, which hinders detailed structural characterization of protein-inhibitor complexes and structural-based inhibitor design. Herein we employed a parallel small molecule library-screening approach to identify inhibitors against three prototype amyloidogenic proteins in neurodegeneration and related proteinopathies: amylin, Aβ and tau. One remarkable class of inhibitors identified from these screens against different amyloidogenic proteins was catechol-containing compounds and redox-related quinones/anthraquinones. Secondary assays validated most of the identified inhibitors. In vivo efficacy evaluation of a selected catechol-containing compound, rosmarinic acid, demonstrated its strong mitigating effects of amylin amyloid deposition and related diabetic pathology in transgenic HIP rats. Further systematic investigation of selected class of inhibitors under aerobic and anaerobic conditions revealed that the redox state of the broad class of catechol-containing compounds is a key determinant of the amyloid inhibitor activities. The molecular insights we gained not only explain why a large number of catechol-containing polyphenolic natural compounds, often enriched in healthy diet, have anti-neurodegeneration and anti-aging activities, but also could guide the rational design of therapeutic or nutraceutical strategies to target a broad range of neurodegenerative and related aging diseases.
[Display omitted]
•Parallel drug library screening identified catechol-containing compounds as a broad class of amyloid inhibitors.•Multiple secondary assays validated most of the identified inhibitors, including in vivo efficacy of rosmarinic acid.•Aerobic but not anaerobic conditions significantly enhanced anti-amyloid activities of the catechol-containing compounds.•Reducing biochemical agents blocked or diminished amyloid remodeling/inhibition activities of catechol-containing inhibitors.•Explain why catechol-containing compounds, enriched in healthy diet, have anti-neurodegeneration and anti-aging effects. |
doi_str_mv | 10.1016/j.phrs.2022.106409 |
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[Display omitted]
•Parallel drug library screening identified catechol-containing compounds as a broad class of amyloid inhibitors.•Multiple secondary assays validated most of the identified inhibitors, including in vivo efficacy of rosmarinic acid.•Aerobic but not anaerobic conditions significantly enhanced anti-amyloid activities of the catechol-containing compounds.•Reducing biochemical agents blocked or diminished amyloid remodeling/inhibition activities of catechol-containing inhibitors.•Explain why catechol-containing compounds, enriched in healthy diet, have anti-neurodegeneration and anti-aging effects.</description><identifier>ISSN: 1043-6618</identifier><identifier>EISSN: 1096-1186</identifier><identifier>DOI: 10.1016/j.phrs.2022.106409</identifier><identifier>PMID: 35995346</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Aggregation modifying inhibitors ; Alzheimer Disease - drug therapy ; Amyloid beta-Peptides - metabolism ; Amyloidogenic Proteins - metabolism ; Animals ; Anthraquinones ; Catechol-containing compounds ; Catechols - pharmacology ; Catechols - therapeutic use ; Diabetes Mellitus, Type 2 ; Drug library screening ; HIP rats ; Islet Amyloid Polypeptide - metabolism ; Islet Amyloid Polypeptide - therapeutic use ; Oxidation-Reduction ; Protein Aggregates ; Protein misfolding diseases ; Quinones ; Rats ; Redox regulation</subject><ispartof>Pharmacological research, 2022-10, Vol.184, p.106409-106409, Article 106409</ispartof><rights>2022 Elsevier Ltd</rights><rights>Copyright © 2022 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-964c4f665b00b15185020dc667489209d322be299d3c2413e190418c139db2693</citedby><cites>FETCH-LOGICAL-c456t-964c4f665b00b15185020dc667489209d322be299d3c2413e190418c139db2693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1043661822003541$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35995346$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Velander, Paul</creatorcontrib><creatorcontrib>Wu, Ling</creatorcontrib><creatorcontrib>Hildreth, Sherry B.</creatorcontrib><creatorcontrib>Vogelaar, Nancy J.</creatorcontrib><creatorcontrib>Mukhopadhyay, Biswarup</creatorcontrib><creatorcontrib>Helm, Richard F.</creatorcontrib><creatorcontrib>Zhang, Shijun</creatorcontrib><creatorcontrib>Xu, Bin</creatorcontrib><title>Catechol-containing compounds are a broad class of protein aggregation inhibitors: Redox state is a key determinant of the inhibitory activities</title><title>Pharmacological research</title><addtitle>Pharmacol Res</addtitle><description>A range of neurodegenerative and related aging diseases, such as Alzheimer’s disease and type 2 diabetes, are linked to toxic protein aggregation. Yet the mechanisms of protein aggregation inhibition by small molecule inhibitors remain poorly understood, in part because most protein targets of aggregation assembly are partially unfolded or intrinsically disordered, which hinders detailed structural characterization of protein-inhibitor complexes and structural-based inhibitor design. Herein we employed a parallel small molecule library-screening approach to identify inhibitors against three prototype amyloidogenic proteins in neurodegeneration and related proteinopathies: amylin, Aβ and tau. One remarkable class of inhibitors identified from these screens against different amyloidogenic proteins was catechol-containing compounds and redox-related quinones/anthraquinones. Secondary assays validated most of the identified inhibitors. In vivo efficacy evaluation of a selected catechol-containing compound, rosmarinic acid, demonstrated its strong mitigating effects of amylin amyloid deposition and related diabetic pathology in transgenic HIP rats. Further systematic investigation of selected class of inhibitors under aerobic and anaerobic conditions revealed that the redox state of the broad class of catechol-containing compounds is a key determinant of the amyloid inhibitor activities. The molecular insights we gained not only explain why a large number of catechol-containing polyphenolic natural compounds, often enriched in healthy diet, have anti-neurodegeneration and anti-aging activities, but also could guide the rational design of therapeutic or nutraceutical strategies to target a broad range of neurodegenerative and related aging diseases.
[Display omitted]
•Parallel drug library screening identified catechol-containing compounds as a broad class of amyloid inhibitors.•Multiple secondary assays validated most of the identified inhibitors, including in vivo efficacy of rosmarinic acid.•Aerobic but not anaerobic conditions significantly enhanced anti-amyloid activities of the catechol-containing compounds.•Reducing biochemical agents blocked or diminished amyloid remodeling/inhibition activities of catechol-containing inhibitors.•Explain why catechol-containing compounds, enriched in healthy diet, have anti-neurodegeneration and anti-aging effects.</description><subject>Aggregation modifying inhibitors</subject><subject>Alzheimer Disease - drug therapy</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Amyloidogenic Proteins - metabolism</subject><subject>Animals</subject><subject>Anthraquinones</subject><subject>Catechol-containing compounds</subject><subject>Catechols - pharmacology</subject><subject>Catechols - therapeutic use</subject><subject>Diabetes Mellitus, Type 2</subject><subject>Drug library screening</subject><subject>HIP rats</subject><subject>Islet Amyloid Polypeptide - metabolism</subject><subject>Islet Amyloid Polypeptide - therapeutic use</subject><subject>Oxidation-Reduction</subject><subject>Protein Aggregates</subject><subject>Protein misfolding diseases</subject><subject>Quinones</subject><subject>Rats</subject><subject>Redox regulation</subject><issn>1043-6618</issn><issn>1096-1186</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kduKFDEQhhtR3IO-gBeSF-jZSjqd6YggMniCBUH0OqSTmu4aZ5ImyQ47b-Ej283oqjdeVVGp_yvCV1UvOKw4cHWzW01jyisBQswDJUE_qi45aFVz3qnHSy-bWineXVRXOe8AQEsOT6uLptW6baS6rH5sbEE3xn3tYiiWAoWBuXiY4l3wmdmEzLI-ReuZ29ucWdyyKcWCFJgdhoSDLRQDozBSTyWm_Ip9QR_vWS4zmdHMYN_xxDwWTAcKNpSFUUb8kzkx6wodqRDmZ9WTrd1nfP6rXlff3r_7uvlY337-8Gnz9rZ2slWl1ko6uVWq7QF63vKuBQHeKbWWnRagfSNEj0LPjROSN8g1SN453mjfC6Wb6-rNmTvd9Qf0DkNJdm-mRAebTiZaMv--BBrNEI-GA6ylXK9ngjgTXIo5J9w-hDmYRZDZmUWQWQSZs6A59PLvsw-R30bmhdfnBZw_fyRMJjvC4NBTQleMj_Q__k_QTqUR</recordid><startdate>20221001</startdate><enddate>20221001</enddate><creator>Velander, Paul</creator><creator>Wu, Ling</creator><creator>Hildreth, Sherry B.</creator><creator>Vogelaar, Nancy J.</creator><creator>Mukhopadhyay, Biswarup</creator><creator>Helm, Richard F.</creator><creator>Zhang, Shijun</creator><creator>Xu, Bin</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20221001</creationdate><title>Catechol-containing compounds are a broad class of protein aggregation inhibitors: Redox state is a key determinant of the inhibitory activities</title><author>Velander, Paul ; Wu, Ling ; Hildreth, Sherry B. ; Vogelaar, Nancy J. ; Mukhopadhyay, Biswarup ; Helm, Richard F. ; Zhang, Shijun ; Xu, Bin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-964c4f665b00b15185020dc667489209d322be299d3c2413e190418c139db2693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Aggregation modifying inhibitors</topic><topic>Alzheimer Disease - drug therapy</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Amyloidogenic Proteins - metabolism</topic><topic>Animals</topic><topic>Anthraquinones</topic><topic>Catechol-containing compounds</topic><topic>Catechols - pharmacology</topic><topic>Catechols - therapeutic use</topic><topic>Diabetes Mellitus, Type 2</topic><topic>Drug library screening</topic><topic>HIP rats</topic><topic>Islet Amyloid Polypeptide - metabolism</topic><topic>Islet Amyloid Polypeptide - therapeutic use</topic><topic>Oxidation-Reduction</topic><topic>Protein Aggregates</topic><topic>Protein misfolding diseases</topic><topic>Quinones</topic><topic>Rats</topic><topic>Redox regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Velander, Paul</creatorcontrib><creatorcontrib>Wu, Ling</creatorcontrib><creatorcontrib>Hildreth, Sherry B.</creatorcontrib><creatorcontrib>Vogelaar, Nancy J.</creatorcontrib><creatorcontrib>Mukhopadhyay, Biswarup</creatorcontrib><creatorcontrib>Helm, Richard F.</creatorcontrib><creatorcontrib>Zhang, Shijun</creatorcontrib><creatorcontrib>Xu, Bin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pharmacological research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Velander, Paul</au><au>Wu, Ling</au><au>Hildreth, Sherry B.</au><au>Vogelaar, Nancy J.</au><au>Mukhopadhyay, Biswarup</au><au>Helm, Richard F.</au><au>Zhang, Shijun</au><au>Xu, Bin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catechol-containing compounds are a broad class of protein aggregation inhibitors: Redox state is a key determinant of the inhibitory activities</atitle><jtitle>Pharmacological research</jtitle><addtitle>Pharmacol Res</addtitle><date>2022-10-01</date><risdate>2022</risdate><volume>184</volume><spage>106409</spage><epage>106409</epage><pages>106409-106409</pages><artnum>106409</artnum><issn>1043-6618</issn><eissn>1096-1186</eissn><abstract>A range of neurodegenerative and related aging diseases, such as Alzheimer’s disease and type 2 diabetes, are linked to toxic protein aggregation. Yet the mechanisms of protein aggregation inhibition by small molecule inhibitors remain poorly understood, in part because most protein targets of aggregation assembly are partially unfolded or intrinsically disordered, which hinders detailed structural characterization of protein-inhibitor complexes and structural-based inhibitor design. Herein we employed a parallel small molecule library-screening approach to identify inhibitors against three prototype amyloidogenic proteins in neurodegeneration and related proteinopathies: amylin, Aβ and tau. One remarkable class of inhibitors identified from these screens against different amyloidogenic proteins was catechol-containing compounds and redox-related quinones/anthraquinones. Secondary assays validated most of the identified inhibitors. In vivo efficacy evaluation of a selected catechol-containing compound, rosmarinic acid, demonstrated its strong mitigating effects of amylin amyloid deposition and related diabetic pathology in transgenic HIP rats. Further systematic investigation of selected class of inhibitors under aerobic and anaerobic conditions revealed that the redox state of the broad class of catechol-containing compounds is a key determinant of the amyloid inhibitor activities. The molecular insights we gained not only explain why a large number of catechol-containing polyphenolic natural compounds, often enriched in healthy diet, have anti-neurodegeneration and anti-aging activities, but also could guide the rational design of therapeutic or nutraceutical strategies to target a broad range of neurodegenerative and related aging diseases.
[Display omitted]
•Parallel drug library screening identified catechol-containing compounds as a broad class of amyloid inhibitors.•Multiple secondary assays validated most of the identified inhibitors, including in vivo efficacy of rosmarinic acid.•Aerobic but not anaerobic conditions significantly enhanced anti-amyloid activities of the catechol-containing compounds.•Reducing biochemical agents blocked or diminished amyloid remodeling/inhibition activities of catechol-containing inhibitors.•Explain why catechol-containing compounds, enriched in healthy diet, have anti-neurodegeneration and anti-aging effects.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>35995346</pmid><doi>10.1016/j.phrs.2022.106409</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aggregation modifying inhibitors Alzheimer Disease - drug therapy Amyloid beta-Peptides - metabolism Amyloidogenic Proteins - metabolism Animals Anthraquinones Catechol-containing compounds Catechols - pharmacology Catechols - therapeutic use Diabetes Mellitus, Type 2 Drug library screening HIP rats Islet Amyloid Polypeptide - metabolism Islet Amyloid Polypeptide - therapeutic use Oxidation-Reduction Protein Aggregates Protein misfolding diseases Quinones Rats Redox regulation |
title | Catechol-containing compounds are a broad class of protein aggregation inhibitors: Redox state is a key determinant of the inhibitory activities |
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