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Biomimetic mimicry of formaldehyde-induced DNA-protein crosslinks in the confined space of a metal-organic framework
DNA-protein crosslinks (DPCs) are highly toxic DNA lesions induced by crosslinking agents such as formaldehyde (HCHO). Building artificial models to simulate the crosslinking process would advance our understanding of the underlying mechanisms and therefore develop coping strategies accordingly. Her...
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Published in: | Chemical science (Cambridge) 2022-05, Vol.13 (17), p.4813-482 |
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creator | Wei, Yu-Bai Luo, Dong Xiong, Xiao Huang, Yong-Liang Xie, Mo Lu, Weigang Li, Dan |
description | DNA-protein crosslinks (DPCs) are highly toxic DNA lesions induced by crosslinking agents such as formaldehyde (HCHO). Building artificial models to simulate the crosslinking process would advance our understanding of the underlying mechanisms and therefore develop coping strategies accordingly. Herein we report the design and synthesis of a Zn-based metal-organic framework with mixed ligands of 2,6-diaminopurine and amine-functionalized dicarboxylate, representing DNA and protein residues, respectively. Combined characterization techniques allow us to demonstrate the unusual efficiency of HCHO-crosslinking within the confined space of the titled MOF. Particularly,
in situ
single-crystal X-ray diffraction studies reveal a sequential methylene-knitting process upon HCHO addition, along with strong fluorescence that was not interfered with by other metabolites, glycine, and Tris. This work has successfully constructed a purine-based metal-organic framework with unoccupied Watson-Crick sites, serving as a crystalline model for HCHO-induced DPCs by mimicking the confinement effect of protein/DNA interactions.
An amine-functionalized biological metal-organic framework serving as a crystalline model for mimicking formaldehyde-induced DNA-protein crosslinks in a confined space. |
doi_str_mv | 10.1039/d2sc00188h |
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in situ
single-crystal X-ray diffraction studies reveal a sequential methylene-knitting process upon HCHO addition, along with strong fluorescence that was not interfered with by other metabolites, glycine, and Tris. This work has successfully constructed a purine-based metal-organic framework with unoccupied Watson-Crick sites, serving as a crystalline model for HCHO-induced DPCs by mimicking the confinement effect of protein/DNA interactions.
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in situ
single-crystal X-ray diffraction studies reveal a sequential methylene-knitting process upon HCHO addition, along with strong fluorescence that was not interfered with by other metabolites, glycine, and Tris. This work has successfully constructed a purine-based metal-organic framework with unoccupied Watson-Crick sites, serving as a crystalline model for HCHO-induced DPCs by mimicking the confinement effect of protein/DNA interactions.
An amine-functionalized biological metal-organic framework serving as a crystalline model for mimicking formaldehyde-induced DNA-protein crosslinks in a confined space.</description><subject>Biomimetics</subject><subject>Chemistry</subject><subject>Confined spaces</subject><subject>Crosslinking</subject><subject>Crystals</subject><subject>Formaldehyde</subject><subject>Glycine</subject><subject>Knitting</subject><subject>Metabolites</subject><subject>Metal-organic frameworks</subject><subject>Mimicry</subject><subject>Proteins</subject><subject>Single crystals</subject><subject>Zinc</subject><issn>2041-6520</issn><issn>2041-6539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpVkc9PHCEUx0mjqUa99N5mEm9NRvkxMHAx0d1Wmxg9tD0Thnm46AysMNtm__uia1fl8iDvkw8v74vQJ4JPCGbqtKfZYkykXHxA-xQ3pBacqZ3tneI9dJTzPS6HMcJp-xHtMS44l0Luo-nCx9GPMHlbleptWlfRVS6m0Qw9LNY91D70Kwt9Nb85r5cpTuBDZVPMefDhIVflNS2gsjE4HwqWl8bCk8RUxWuGOqY7E4rfJTPC35geDtGuM0OGo5d6gH5___ZrdlVf317-mJ1f15ZxOdWsIaBYqzrMsWPYSGt5JwAwdcyyVrCO0K4VipheQOcwNNARK2lDKJWqlewAnW28y1U3Qm8hTMkMepn8aNJaR-P1-07wC30X_2iFRcsVKYLjF0GKjyvIk76PqxTKzJoKrmjZZkML9XVDPS8lgdv-QLB-CknP6c_Zc0hXBf7ydqYt-j-SAnzeACnbbfc1ZfYPe_uYZQ</recordid><startdate>20220504</startdate><enddate>20220504</enddate><creator>Wei, Yu-Bai</creator><creator>Luo, Dong</creator><creator>Xiong, Xiao</creator><creator>Huang, Yong-Liang</creator><creator>Xie, Mo</creator><creator>Lu, Weigang</creator><creator>Li, Dan</creator><general>Royal Society of Chemistry</general><general>The 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>5PM</scope><orcidid>https://orcid.org/0000-0001-9751-8241</orcidid><orcidid>https://orcid.org/0000-0001-6721-3711</orcidid><orcidid>https://orcid.org/0000-0002-0433-0328</orcidid><orcidid>https://orcid.org/0000-0003-1569-014X</orcidid><orcidid>https://orcid.org/0000-0002-0661-5044</orcidid><orcidid>https://orcid.org/0000-0001-6960-4783</orcidid><orcidid>https://orcid.org/0000-0002-4936-4599</orcidid></search><sort><creationdate>20220504</creationdate><title>Biomimetic mimicry of formaldehyde-induced DNA-protein crosslinks in the confined space of a metal-organic framework</title><author>Wei, Yu-Bai ; Luo, Dong ; Xiong, Xiao ; Huang, Yong-Liang ; Xie, Mo ; Lu, Weigang ; Li, Dan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-341e9379b050f30a8cc5b6ee02f3c3763b12b7691ad6ebf0e4eb1c82412289783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biomimetics</topic><topic>Chemistry</topic><topic>Confined spaces</topic><topic>Crosslinking</topic><topic>Crystals</topic><topic>Formaldehyde</topic><topic>Glycine</topic><topic>Knitting</topic><topic>Metabolites</topic><topic>Metal-organic frameworks</topic><topic>Mimicry</topic><topic>Proteins</topic><topic>Single crystals</topic><topic>Zinc</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wei, Yu-Bai</creatorcontrib><creatorcontrib>Luo, Dong</creatorcontrib><creatorcontrib>Xiong, Xiao</creatorcontrib><creatorcontrib>Huang, Yong-Liang</creatorcontrib><creatorcontrib>Xie, Mo</creatorcontrib><creatorcontrib>Lu, Weigang</creatorcontrib><creatorcontrib>Li, Dan</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>PubMed Central (Full Participant titles)</collection><jtitle>Chemical science (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wei, Yu-Bai</au><au>Luo, Dong</au><au>Xiong, Xiao</au><au>Huang, Yong-Liang</au><au>Xie, Mo</au><au>Lu, Weigang</au><au>Li, Dan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biomimetic mimicry of formaldehyde-induced DNA-protein crosslinks in the confined space of a metal-organic framework</atitle><jtitle>Chemical science (Cambridge)</jtitle><addtitle>Chem Sci</addtitle><date>2022-05-04</date><risdate>2022</risdate><volume>13</volume><issue>17</issue><spage>4813</spage><epage>482</epage><pages>4813-482</pages><issn>2041-6520</issn><eissn>2041-6539</eissn><abstract>DNA-protein crosslinks (DPCs) are highly toxic DNA lesions induced by crosslinking agents such as formaldehyde (HCHO). Building artificial models to simulate the crosslinking process would advance our understanding of the underlying mechanisms and therefore develop coping strategies accordingly. Herein we report the design and synthesis of a Zn-based metal-organic framework with mixed ligands of 2,6-diaminopurine and amine-functionalized dicarboxylate, representing DNA and protein residues, respectively. Combined characterization techniques allow us to demonstrate the unusual efficiency of HCHO-crosslinking within the confined space of the titled MOF. Particularly,
in situ
single-crystal X-ray diffraction studies reveal a sequential methylene-knitting process upon HCHO addition, along with strong fluorescence that was not interfered with by other metabolites, glycine, and Tris. This work has successfully constructed a purine-based metal-organic framework with unoccupied Watson-Crick sites, serving as a crystalline model for HCHO-induced DPCs by mimicking the confinement effect of protein/DNA interactions.
An amine-functionalized biological metal-organic framework serving as a crystalline model for mimicking formaldehyde-induced DNA-protein crosslinks in a confined space.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>35655868</pmid><doi>10.1039/d2sc00188h</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-9751-8241</orcidid><orcidid>https://orcid.org/0000-0001-6721-3711</orcidid><orcidid>https://orcid.org/0000-0002-0433-0328</orcidid><orcidid>https://orcid.org/0000-0003-1569-014X</orcidid><orcidid>https://orcid.org/0000-0002-0661-5044</orcidid><orcidid>https://orcid.org/0000-0001-6960-4783</orcidid><orcidid>https://orcid.org/0000-0002-4936-4599</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biomimetics Chemistry Confined spaces Crosslinking Crystals Formaldehyde Glycine Knitting Metabolites Metal-organic frameworks Mimicry Proteins Single crystals Zinc |
title | Biomimetic mimicry of formaldehyde-induced DNA-protein crosslinks in the confined space of a metal-organic framework |
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