Programed Assembly of Nucleoprotein Nanoparticles Using DNA and Zinc Fingers for Targeted Protein Delivery
With a growing number of intracellular drug targets and the high efficacy of protein therapeutics, the targeted delivery of active proteins with negligible toxicity is a challenging issue in the field of precision medicine. Herein, a programed assembly of nucleoprotein nanoparticles (NNPs) using DNA...
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creator | Ryu, Yiseul Kang, Jung Ae Kim, Dasom Kim, Song‐Rae Kim, Seungmin Park, Seong Ji Kwon, Seung‐Hae Kim, Kil‐Nam Lee, Dong‐Eun Lee, Joong‐jae Kim, Hak‐Sung |
description | With a growing number of intracellular drug targets and the high efficacy of protein therapeutics, the targeted delivery of active proteins with negligible toxicity is a challenging issue in the field of precision medicine. Herein, a programed assembly of nucleoprotein nanoparticles (NNPs) using DNA and zinc fingers (ZnFs) for targeted protein delivery is presented. Two types of ZnFs with different sequence specificities are genetically fused to a targeting moiety and a protein cargo, respectively. Double‐stranded DNA with multiple ZnF‐binding sequences is grafted onto inorganic nanoparticles, followed by conjugation with the ZnF‐fused proteins, generating the assembly of NNPs with a uniform size distribution and high stability. The approach enables controlled loading of a protein cargo on the NNPs, offering a high cytosolic delivery efficiency and target specificity. The utility and potential of the assembly as a versatile protein delivery vehicle is demonstrated based on their remarkable antitumor activity and target specificity with negligible toxicity in a xenograft mice model.
Nucleoprotein nanoparticles (NNPs) are assembled through specific interactions between zinc fingers and template DNAs on gold nanoparticles for targeted protein delivery. With controlled loading of a cytotoxic protein, the NNPs show a remarkable antitumor activity in xenograft mice. The NNPs find wide applications in biological and medical sciences. |
doi_str_mv | 10.1002/smll.201802618 |
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Nucleoprotein nanoparticles (NNPs) are assembled through specific interactions between zinc fingers and template DNAs on gold nanoparticles for targeted protein delivery. With controlled loading of a cytotoxic protein, the NNPs show a remarkable antitumor activity in xenograft mice. The NNPs find wide applications in biological and medical sciences.</description><identifier>ISSN: 1613-6810</identifier><identifier>EISSN: 1613-6829</identifier><identifier>DOI: 10.1002/smll.201802618</identifier><identifier>PMID: 30398698</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Anticancer properties ; Assembly ; Conjugation ; Control stability ; Deoxyribonucleic acid ; DNA ; Drug delivery systems ; Gene sequencing ; Nanoparticles ; Nanotechnology ; nucleoproteins ; protein delivery ; Proteins ; self‐assembly ; Size distribution ; targeted therapy ; Toxicity ; Xenotransplantation ; Zinc</subject><ispartof>Small (Weinheim an der Bergstrasse, Germany), 2018-12, Vol.14 (52), p.e1802618-n/a</ispartof><rights>2018 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3738-72d9aaa630f8db8d4606cff03bbe7432af544d9424623493aa2b1d8046bf03dd3</citedby><cites>FETCH-LOGICAL-c3738-72d9aaa630f8db8d4606cff03bbe7432af544d9424623493aa2b1d8046bf03dd3</cites><orcidid>0000-0002-3121-1420</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fsmll.201802618$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fsmll.201802618$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30398698$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ryu, Yiseul</creatorcontrib><creatorcontrib>Kang, Jung Ae</creatorcontrib><creatorcontrib>Kim, Dasom</creatorcontrib><creatorcontrib>Kim, Song‐Rae</creatorcontrib><creatorcontrib>Kim, Seungmin</creatorcontrib><creatorcontrib>Park, Seong Ji</creatorcontrib><creatorcontrib>Kwon, Seung‐Hae</creatorcontrib><creatorcontrib>Kim, Kil‐Nam</creatorcontrib><creatorcontrib>Lee, Dong‐Eun</creatorcontrib><creatorcontrib>Lee, Joong‐jae</creatorcontrib><creatorcontrib>Kim, Hak‐Sung</creatorcontrib><title>Programed Assembly of Nucleoprotein Nanoparticles Using DNA and Zinc Fingers for Targeted Protein Delivery</title><title>Small (Weinheim an der Bergstrasse, Germany)</title><addtitle>Small</addtitle><description>With a growing number of intracellular drug targets and the high efficacy of protein therapeutics, the targeted delivery of active proteins with negligible toxicity is a challenging issue in the field of precision medicine. Herein, a programed assembly of nucleoprotein nanoparticles (NNPs) using DNA and zinc fingers (ZnFs) for targeted protein delivery is presented. Two types of ZnFs with different sequence specificities are genetically fused to a targeting moiety and a protein cargo, respectively. Double‐stranded DNA with multiple ZnF‐binding sequences is grafted onto inorganic nanoparticles, followed by conjugation with the ZnF‐fused proteins, generating the assembly of NNPs with a uniform size distribution and high stability. The approach enables controlled loading of a protein cargo on the NNPs, offering a high cytosolic delivery efficiency and target specificity. The utility and potential of the assembly as a versatile protein delivery vehicle is demonstrated based on their remarkable antitumor activity and target specificity with negligible toxicity in a xenograft mice model.
Nucleoprotein nanoparticles (NNPs) are assembled through specific interactions between zinc fingers and template DNAs on gold nanoparticles for targeted protein delivery. With controlled loading of a cytotoxic protein, the NNPs show a remarkable antitumor activity in xenograft mice. The NNPs find wide applications in biological and medical sciences.</description><subject>Anticancer properties</subject><subject>Assembly</subject><subject>Conjugation</subject><subject>Control stability</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Drug delivery systems</subject><subject>Gene sequencing</subject><subject>Nanoparticles</subject><subject>Nanotechnology</subject><subject>nucleoproteins</subject><subject>protein delivery</subject><subject>Proteins</subject><subject>self‐assembly</subject><subject>Size distribution</subject><subject>targeted therapy</subject><subject>Toxicity</subject><subject>Xenotransplantation</subject><subject>Zinc</subject><issn>1613-6810</issn><issn>1613-6829</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkM9LwzAYQIMobk6vHiXguTO_TJPjmE6FOgduFy8lbdLR0TYzaZX-92ZszqOnhI_3vYQHwDVGY4wQufN1VY0JwgIRjsUJGGKOacQFkafHO0YDcOH9BiGKCYvPwYAiKgWXYgg2C2fXTtVGw4n3ps6qHtoCzru8MnbrbGvKBs5VY7fKtWUYerjyZbOGD_MJVI2GH2WTw1mYGOdhYR1cKrc2bfAtDtsPpiq_jOsvwVmhKm-uDucIrGaPy-lzlLw9vUwnSZTTmIooJloqpThFhdCZ0IwjnhcFollmYkaJKu4Z05IRxgllkipFMqwFYjwLkNZ0BG733vD9z874Nt3YzjXhyZTgIJOEsThQ4z2VO-u9M0W6dWWtXJ9ilO7Spru06TFtWLg5aLss5Drivy0DIPfAd1mZ_h9d-v6aJH_yH1P1hj0</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Ryu, Yiseul</creator><creator>Kang, Jung Ae</creator><creator>Kim, Dasom</creator><creator>Kim, Song‐Rae</creator><creator>Kim, Seungmin</creator><creator>Park, Seong Ji</creator><creator>Kwon, Seung‐Hae</creator><creator>Kim, Kil‐Nam</creator><creator>Lee, Dong‐Eun</creator><creator>Lee, Joong‐jae</creator><creator>Kim, Hak‐Sung</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-3121-1420</orcidid></search><sort><creationdate>201812</creationdate><title>Programed Assembly of Nucleoprotein Nanoparticles Using DNA and Zinc Fingers for Targeted Protein Delivery</title><author>Ryu, Yiseul ; Kang, Jung Ae ; Kim, Dasom ; Kim, Song‐Rae ; Kim, Seungmin ; Park, Seong Ji ; Kwon, Seung‐Hae ; Kim, Kil‐Nam ; Lee, Dong‐Eun ; Lee, Joong‐jae ; Kim, Hak‐Sung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3738-72d9aaa630f8db8d4606cff03bbe7432af544d9424623493aa2b1d8046bf03dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Anticancer properties</topic><topic>Assembly</topic><topic>Conjugation</topic><topic>Control stability</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Drug delivery systems</topic><topic>Gene sequencing</topic><topic>Nanoparticles</topic><topic>Nanotechnology</topic><topic>nucleoproteins</topic><topic>protein delivery</topic><topic>Proteins</topic><topic>self‐assembly</topic><topic>Size distribution</topic><topic>targeted therapy</topic><topic>Toxicity</topic><topic>Xenotransplantation</topic><topic>Zinc</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ryu, Yiseul</creatorcontrib><creatorcontrib>Kang, Jung Ae</creatorcontrib><creatorcontrib>Kim, Dasom</creatorcontrib><creatorcontrib>Kim, Song‐Rae</creatorcontrib><creatorcontrib>Kim, Seungmin</creatorcontrib><creatorcontrib>Park, Seong Ji</creatorcontrib><creatorcontrib>Kwon, Seung‐Hae</creatorcontrib><creatorcontrib>Kim, Kil‐Nam</creatorcontrib><creatorcontrib>Lee, Dong‐Eun</creatorcontrib><creatorcontrib>Lee, Joong‐jae</creatorcontrib><creatorcontrib>Kim, Hak‐Sung</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ryu, Yiseul</au><au>Kang, Jung Ae</au><au>Kim, Dasom</au><au>Kim, Song‐Rae</au><au>Kim, Seungmin</au><au>Park, Seong Ji</au><au>Kwon, Seung‐Hae</au><au>Kim, Kil‐Nam</au><au>Lee, Dong‐Eun</au><au>Lee, Joong‐jae</au><au>Kim, Hak‐Sung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Programed Assembly of Nucleoprotein Nanoparticles Using DNA and Zinc Fingers for Targeted Protein Delivery</atitle><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle><addtitle>Small</addtitle><date>2018-12</date><risdate>2018</risdate><volume>14</volume><issue>52</issue><spage>e1802618</spage><epage>n/a</epage><pages>e1802618-n/a</pages><issn>1613-6810</issn><eissn>1613-6829</eissn><abstract>With a growing number of intracellular drug targets and the high efficacy of protein therapeutics, the targeted delivery of active proteins with negligible toxicity is a challenging issue in the field of precision medicine. Herein, a programed assembly of nucleoprotein nanoparticles (NNPs) using DNA and zinc fingers (ZnFs) for targeted protein delivery is presented. Two types of ZnFs with different sequence specificities are genetically fused to a targeting moiety and a protein cargo, respectively. Double‐stranded DNA with multiple ZnF‐binding sequences is grafted onto inorganic nanoparticles, followed by conjugation with the ZnF‐fused proteins, generating the assembly of NNPs with a uniform size distribution and high stability. The approach enables controlled loading of a protein cargo on the NNPs, offering a high cytosolic delivery efficiency and target specificity. The utility and potential of the assembly as a versatile protein delivery vehicle is demonstrated based on their remarkable antitumor activity and target specificity with negligible toxicity in a xenograft mice model.
Nucleoprotein nanoparticles (NNPs) are assembled through specific interactions between zinc fingers and template DNAs on gold nanoparticles for targeted protein delivery. With controlled loading of a cytotoxic protein, the NNPs show a remarkable antitumor activity in xenograft mice. The NNPs find wide applications in biological and medical sciences.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30398698</pmid><doi>10.1002/smll.201802618</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-3121-1420</orcidid></addata></record> |
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subjects | Anticancer properties Assembly Conjugation Control stability Deoxyribonucleic acid DNA Drug delivery systems Gene sequencing Nanoparticles Nanotechnology nucleoproteins protein delivery Proteins self‐assembly Size distribution targeted therapy Toxicity Xenotransplantation Zinc |
title | Programed Assembly of Nucleoprotein Nanoparticles Using DNA and Zinc Fingers for Targeted Protein Delivery |
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