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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Veröffentlicht in:Small (Weinheim an der Bergstrasse, Germany) Germany), 2018-12, Vol.14 (52), p.e1802618-n/a
Hauptverfasser: 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
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container_issue 52
container_start_page e1802618
container_title Small (Weinheim an der Bergstrasse, Germany)
container_volume 14
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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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. 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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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