Prospects and challenges of dynamic DNA nanostructures in biomedical applications

Taoran Tian , Yanjing Li , Yunfeng Lin

Bone Research ›› 2022, Vol. 10 ›› Issue (1) : 40

PDF
Bone Research ›› 2022, Vol. 10 ›› Issue (1) : 40 DOI: 10.1038/s41413-022-00212-1
Review Article

Prospects and challenges of dynamic DNA nanostructures in biomedical applications

Author information +
History +
PDF

Abstract

The physicochemical nature of DNA allows the assembly of highly predictable structures via several fabrication strategies, which have been applied to make breakthroughs in various fields. Moreover, DNA nanostructures are regarded as materials with excellent editability and biocompatibility for biomedical applications. The ongoing maintenance and release of new DNA structure design tools ease the work and make large and arbitrary DNA structures feasible for different applications. However, the nature of DNA nanostructures endows them with several stimulus-responsive mechanisms capable of responding to biomolecules, such as nucleic acids and proteins, as well as biophysical environmental parameters, such as temperature and pH. Via these mechanisms, stimulus-responsive dynamic DNA nanostructures have been applied in several biomedical settings, including basic research, active drug delivery, biosensor development, and tissue engineering. These applications have shown the versatility of dynamic DNA nanostructures, with unignorable merits that exceed those of their traditional counterparts, such as polymers and metal particles. However, there are stability, yield, exogenous DNA, and ethical considerations regarding their clinical translation. In this review, we first introduce the recent efforts and discoveries in DNA nanotechnology, highlighting the uses of dynamic DNA nanostructures in biomedical applications. Then, several dynamic DNA nanostructures are presented, and their typical biomedical applications, including their use as DNA aptamers, ion concentration/pH-sensitive DNA molecules, DNA nanostructures capable of strand displacement reactions, and protein-based dynamic DNA nanostructures, are discussed. Finally, the challenges regarding the biomedical applications of dynamic DNA nanostructures are discussed.

Cite this article

Download citation ▾
Taoran Tian, Yanjing Li, Yunfeng Lin. Prospects and challenges of dynamic DNA nanostructures in biomedical applications. Bone Research, 2022, 10(1): 40 DOI:10.1038/s41413-022-00212-1

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Seeman NC. DNA in a material world. Nature, 2003, 421: 427-431

[2]

Winfree E, Liu F, Wenzler LA, Seeman NC. Design and self-assembly of two-dimensional DNA crystals. Nature, 1998, 394: 539-544

[3]

Seeman NC, Sleiman HF. DNA nanotechnology. Nat. Rev. Mater., 2017, 3: 17068

[4]

Pinheiro AV, Han D, Shih WM, Yan H. Challenges and opportunities for structural DNA nanotechnology. Nat. Nanotechnol., 2011, 6: 763-772

[5]

Mathieu F et al. Six-helix bundles designed from DNA. Nano Lett., 2005, 5: 661-665

[6]

Vinogradov AE. DNA helix: the importance of being GC‐rich. Nucleic Acids Res., 2003, 31: 1838-1844

[7]

Goodman, R. P., Berry, R. M. & Turberfield, A. J. The single-step synthesis of a DNA tetrahedron. Chem. Commun. 1372–1373 (2004).

[8]

Goodman RP et al. Reconfigurable, braced, three-dimensional DNA nanostructures. Nat. Nanotechnol., 2008, 3: 93-96

[9]

Yan H, LaBean TH, Feng L, Reif JH. Directed nucleation assembly of DNA tile complexes for barcode-patterned lattices. Proc. Natl. Acad. Sci. USA, 2003, 100: 8103-8108

[10]

Lin C, Liu Y, Rinker S, Yan H. DNA tile based self‐assembly: building complex nanoarchitectures. ChemPhysChem, 2006, 7: 1641-1647

[11]

Nummelin S, Kommeri J, Kostiainen MA, Linko V. Evolution of Structural DNA Nanotechnology. Adv. Mater., 2018, 30: e1703721

[12]

Douglas SM et al. Rapid prototyping of 3D DNA-origami shapes with caDNAno. Nucleic Acids Res., 2009, 37: 5001-5006

[13]

Williams, S. et al. In International Workshop on DNA-based Computers. 90-101 (Springer).

[14]

Zadeh JN et al. NUPACK: Analysis and design of nucleic acid systems. J. Comput. Chem., 2011, 32: 170-173

[15]

Kim DN, Kilchherr F, Dietz H, Bathe M. Quantitative prediction of 3D solution shape and flexibility of nucleic acid nanostructures. Nucleic acids Res., 2012, 40: 2862-2868

[16]

Doye, J. P. et al. The oxDNA coarse-grained model as a tool to simulate DNA origami. arXiv preprint arXiv:2004.05052. (2020).

[17]

Castro CE et al. A primer to scaffolded DNA origami. Nat. Methods, 2011, 8: 221

[18]

Zhang F et al. Complex wireframe DNA origami nanostructures with multi-arm junction vertices. Nat. Nanotechnol., 2015, 10: 779

[19]

Zhou Z, Zhang P, Yue L, Willner I. Triggered interconversion of dynamic networks composed of DNA-Tetrahedra nanostructures. Nano Lett., 2019, 19: 7540-7547

[20]

Tikhomirov G, Petersen P, Qian L. Fractal assembly of micrometre-scale DNA origami arrays with arbitrary patterns. Nature, 2017, 552: 67-71

[21]

Zhang DY, Seelig G. Dynamic DNA nanotechnology using strand-displacement reactions. Nat. Chem., 2011, 3: 103-113

[22]

Ramezani H, Dietz H. Building machines with DNA molecules. Nat. Rev. Genet., 2020, 21: 5-26

[23]

Ma W et al. The biological applications of DNA nanomaterials: current challenges and future directions. Signal Transduct. Target Ther., 2021, 6: 351

[24]

Zhang T et al. Design, fabrication and applications of tetrahedral DNA nanostructure-based multifunctional complexes in drug delivery and biomedical treatment. Nat. Protoc., 2020, 15: 2728-2757

[25]

Li J et al. The neuroprotective effect of MicroRNA‐22‐3p modified tetrahedral framework nucleic acids on damaged retinal neurons via TrkB/BDNF signaling pathway. Adv. Funct. Mater., 2021, 31: 2104141

[26]

Li Y et al. Tetrahedral framework nucleic acid-based delivery of resveratrol alleviates insulin resistance: From innate to adaptive immunity. Nanomicro Lett., 2021, 13: 86

[27]

Zhang M et al. Anti-inflammatory activity of curcumin-loaded tetrahedral framework nucleic acids on acute gouty arthritis. Bioact. Mater., 2022, 8: 368-380

[28]

Wang Y et al. Tetrahedral framework nucleic acids can alleviate taurocholate-induced severe acute pancreatitis and its subsequent multiorgan injury in mice. Nano Lett., 2022, 22: 1759-1768

[29]

Zhou Y et al. An organelle-specific nanozyme for diabetes care in genetically or diet-induced models. Adv. Mater., 2020, 32: 2003708

[30]

Shen H, Wang Y, Wang J, Li Z, Yuan Q. Emerging biomimetic applications of DNA nanotechnology. ACS Appl. Mater. Interfaces, 2019, 11: 13859-13873

[31]

Liu L et al. Efficient and reliable MicroRNA imaging in living cells via a FRET-based localized Hairpin-DNA cascade amplifier. Anal. Chem., 2019, 91: 3675-3680

[32]

Burns JR, Seifert A, Fertig N, Howorka S. A biomimetic DNA-based channel for the ligand-controlled transport of charged molecular cargo across a biological membrane. Nat. Nanotechnol., 2016, 11: 152-156

[33]

Fisher PDE et al. A programmable DNA origami platform for organizing intrinsically disordered nucleoporins within nanopore confinement. ACS Nano, 2018, 12: 1508-1518

[34]

Shen Q et al. DNA-origami nanotrap for studying the selective barriers formed by phenylalanine-glycine-rich nucleoporins. J. Am. Chem. Soc., 2021, 143: 12294-12303

[35]

Woods D et al. Diverse and robust molecular algorithms using reprogrammable DNA self-assembly. Nature, 2019, 567: 366-372

[36]

Li S et al. A DNA nanorobot functions as a cancer therapeutic in response to a molecular trigger in vivo. Nat. Biotechnol., 2018, 36: 258-264

[37]

Liu S et al. A DNA nanodevice-based vaccine for cancer immunotherapy. Nat. Mater., 2021, 20: 421-430

[38]

Kahn JS, Hu Y, Willner I. Stimuli-responsive DNA-based hydrogels: from basic principles to applications. Acc. Chem. Res, 2017, 50: 680-690

[39]

Zhang J, Song S, Wang L, Pan D, Fan C. A gold nanoparticle-based chronocoulometric DNA sensor for amplified detection of DNA. Nat. Protoc., 2007, 2: 2888-2895

[40]

Wagenbauer KF, Sigl C, Dietz H. Gigadalton-scale shape-programmable DNA assemblies. Nature, 2017, 552: 78-83

[41]

Ong LL et al. Programmable self-assembly of three-dimensional nanostructures from 10,000 unique components. Nature, 2017, 552: 72-77

[42]

Praetorius F et al. Biotechnological mass production of DNA origami. Nature, 2017, 552: 84-87

[43]

Modi S et al. A DNA nanomachine that maps spatial and temporal pH changes inside living cells. Nat. Nanotechnol., 2009, 4: 325-330

[44]

Du Y, Peng P, Li T. DNA logic operations in living cells utilizing lysosome-recognizing framework nucleic acid nanodevices for subcellular imaging. ACS Nano, 2019, 13: 5778-5784

[45]

Fong FY, Oh SS, Hawker CJ, Soh HT. In vitro selection of pH-activated DNA nanostructures. Angew. Chem. Int Ed. Engl., 2016, 55: 15258-15262

[46]

Kim SH et al. Reversible regulation of enzyme activity by ph-responsive encapsulation in DNA nanocages. ACS Nano, 2017, 11: 9352-9359

[47]

Ijas H, Hakaste I, Shen B, Kostiainen MA, Linko V. Reconfigurable DNA Origami nanocapsule for pH-controlled encapsulation and display of cargo. ACS Nano, 2019, 13: 5959-5967

[48]

Andersen ES et al. Self-assembly of a nanoscale DNA box with a controllable lid. Nature, 2009, 459: 73-76

[49]

Li Q et al. Aptamer-modified tetrahedral DNA nanostructure for tumor-targeted drug delivery. ACS Appl Mater. Interfaces, 2017, 9: 36695-36701

[50]

Xing C et al. Active self-assembly of train-shaped DNA nanostructures via catalytic hairpin assembly reactions. Small, 2019, 15: e1901795

[51]

Wu H, Chen TT, Wang XN, Ke Y, Jiang JH. RNA imaging in living mice enabled by an in vivo hybridization chain reaction circuit with a tripartite DNA probe. Chem. Sci., 2020, 11: 62-69

[52]

Juul S et al. Temperature-controlled encapsulation and release of an active enzyme in the cavity of a self-assembled DNA nanocage. ACS Nano, 2013, 7: 9724-9734

[53]

Kim CJ, Jeong EH, Lee H, Park SJ. A dynamic DNA nanostructure with switchable and size-selective molecular recognition properties. Nanoscale, 2019, 11: 2501-2509

[54]

Zhang L et al. Engineering of bioinspired, size-controllable, self-degradable cancer-targeting DNA nanoflowers via the incorporation of an artificial sandwich base. J. Am. Chem. Soc., 2019, 141: 4282-4290

[55]

Shen C, Liu S, Li X, Yang M. Electrochemical detection of circulating tumor cells based on DNA generated electrochemical current and rolling circle amplification. Anal. Chem., 2019, 91: 11614-11619

[56]

Gao H, Zhang K, Teng X, Li J. Rolling circle amplification for single cell analysis and in situ sequencing. TrAC Trends Anal. Chem., 2019, 121: 115700

[57]

Sharma VK, Watts JK. Oligonucleotide therapeutics: chemistry, delivery and clinical progress. Future Med. Chem., 2015, 7: 2221-2242

[58]

Sefah K, Shangguan D, Xiong X, O’Donoghue MB, Tan W. Development of DNA aptamers using Cell-SELEX. Nat. Protoc., 2010, 5: 1169-1185

[59]

Xing H, Wong NY, Xiang Y, Lu Y. DNA aptamer functionalized nanomaterials for intracellular analysis, cancer cell imaging and drug delivery. Curr. Opin. Chem. Biol., 2012, 16: 429-435

[60]

Hirao I, Kimoto M, Lee KH. DNA aptamer generation by ExSELEX using genetic alphabet expansion with a mini-hairpin DNA stabilization method. Biochimie, 2018, 145: 15-21

[61]

Cansiz S et al. DNA Aptamer based nanodrugs: Molecular engineering for efficiency. Chem. Asian J., 2015, 10: 2084-2094

[62]

Kimoto M, Nakamura M, Hirao I. Post-ExSELEX stabilization of an unnatural-base DNA aptamer targeting VEGF165 toward pharmaceutical applications. Nucleic Acids Res., 2016, 44: 7487-7494

[63]

Christian S et al. Nucleolin expressed at the cell surface is a marker of endothelial cells in angiogenic blood vessels. J. cell Biol., 2003, 163: 871-878

[64]

Keefe AD, Pai S, Ellington A. Aptamers as therapeutics. Nat. Rev. Drug Discov., 2010, 9: 537-550

[65]

Bunka DH, Platonova O, Stockley PG. Development of aptamer therapeutics. Curr. Opin. Pharm., 2010, 10: 557-562

[66]

Han Y et al. Immune lipoprotein nanostructures inspired relay drug delivery for amplifying antitumor efficiency. Biomaterials, 2018, 185: 205-218

[67]

Kohwi Y, Kohwi-Shigematsu T. Magnesium ion-dependent triple-helix structure formed by homopurine-homopyrimidine sequences in supercoiled plasmid DNA. Proc. Natl. Acad. Sci. USA, 1988, 85: 3781-3785

[68]

Wu YY, Zhang ZL, Zhang JS, Zhu XL, Tan ZJ. Multivalent ion-mediated nucleic acid helix-helix interactions: RNA versus DNA. Nucleic acids Res., 2015, 43: 6156-6165

[69]

Takezawa Y, Müller J, Shionoya M. Artificial DNA base pairing mediated by diverse metal ions. Chem. Lett., 2017, 46: 622-633

[70]

Zhang ZL, Wu YY, Xi K, Sang JP, Tan ZJ. Divalent ion-mediated DNA-DNA interactions: A comparative study of triplex and duplex. Biophys. J., 2017, 113: 517-528

[71]

Naskar S, Guha R, Muller J. Metal-modified nucleic acids: Metal-mediated base pairs, triples, and tetrads. Angew. Chem. Int. Ed. Engl., 2020, 59: 1397-1406

[72]

Guo K et al. Formation of pseudosymmetrical G-quadruplex and i-motif structures in the proximal promoter region of the RET oncogene. J. Am. Chem. Soc., 2007, 129: 10220-10228

[73]

Chu B, Zhang D, Paukstelis PJ. A DNA G-quadruplex/i-motif hybrid. Nucleic Acids Res., 2019, 47: 11921-11930

[74]

Zhang Z et al. Acidic pH environment induces autophagy in osteoblasts. Sci. Rep., 2017, 7

[75]

Galow AM et al. Increased osteoblast viability at alkaline pH in vitro provides a new perspective on bone regeneration. Biochem. Biophys. Rep., 2017, 10: 17-25

[76]

Skolakova P et al. Systematic investigation of sequence requirements for DNA i-motif formation. Nucleic Acids Res., 2019, 47: 2177-2189

[77]

Abou Assi H, Garavis M, Gonzalez C, Damha MJ. i-Motif DNA: Structural features and significance to cell biology. Nucleic Acids Res., 2018, 46: 8038-8056

[78]

Park H, Kim J, Jung S, Kim WJ. DNA‐Au nanomachine equipped with i‐Motif and G‐Quadruplex for triple combinatorial anti‐tumor therapy. Adv. Funct. Mater., 2018, 28: 1705416

[79]

Keum JW, Bermudez H. DNA-based delivery vehicles: pH-controlled disassembly and cargo release. Chem. Commun. (Camb.), 2012, 48: 12118-12120

[80]

Ma W et al. I-Motif-based in situ bipedal hybridization chain reaction for specific activatable imaging and enhanced delivery of antisense oligonucleotides. Anal. Chem., 2019, 91: 12538-12545

[81]

Liu H et al. Kinetics of RNA and RNA:DNA hybrid strand displacement. ACS Synth. Biol., 2021, 10: 3066-3073

[82]

Qian L, Winfree E. Scaling up digital circuit computation with DNA strand displacement cascades. Science, 2011, 332: 1196-1201

[83]

Figg CA, Winegar PH, Hayes OG, Mirkin CA. Controlling the DNA hybridization chain reaction. J. Am. Chem. Soc., 2020, 142: 8596-8601

[84]

Dirks RM, Pierce NA. Triggered amplification by hybridization chain reaction. Proc. Natl. Acad. Sci. USA, 2004, 101: 15275-15278

[85]

Li B, Ellington AD, Chen X. Rational, modular adaptation of enzyme-free DNA circuits to multiple detection methods. Nucleic Acids Res., 2011, 39: e110

[86]

Chen J, Wen J, Zhuang L, Zhou S. An enzyme-free catalytic DNA circuit for amplified detection of aflatoxin B1 using gold nanoparticles as colorimetric indicators. Nanoscale, 2016, 8: 9791-9797

[87]

Zhou F et al. Proximity hybridization-regulated catalytic DNA hairpin assembly for electrochemical immunoassay based on in situ DNA template-synthesized Pd nanoparticles. Anal. Chim. Acta, 2017, 969: 8-17

[88]

Wei Q et al. A DNA nanowire based localized catalytic hairpin assembly reaction for microRNA imaging in live cells. Chem. Sci., 2018, 9: 7802-7808

[89]

Tang J et al. Recognition-driven remodeling of dual-split aptamer triggering in situ hybridization chain reaction for activatable and autonomous identification of cancer cells. Anal. Chem., 2020, 92: 10839-10846

[90]

Yao C et al. Double rolling circle amplification generates physically cross-linked DNA network for stem cell fishing. J. Am. Chem. Soc., 2020, 142: 3422-3429

[91]

Guo Q et al. DNA-based hybridization chain reaction and biotin-streptavidin signal amplification for sensitive detection of Escherichia coli O157:H7 through ELISA. Biosens. Bioelectron., 2016, 86: 990-995

[92]

Tang Y et al. Universal strategy to engineer catalytic DNA hairpin assemblies for protein analysis. Anal. Chem., 2015, 87: 8063-8066

[93]

Yang L, Fung CW, Cho EJ, Ellington AD. Real-time rolling circle amplification for protein detection. Anal. Chem., 2007, 79: 3320-3329

[94]

Lizardi PM et al. Mutation detection and single-molecule counting using isothermal rolling-circle amplification. Nat. Genet., 1998, 19: 225-232

[95]

Ciftci S et al. Digital rolling circle amplification-based detection of ebola and other tropical viruses. J. Mol. Diagn., 2020, 22: 272-283

[96]

Zhao, Y. et al. Nucleic Acids Analysis. Sci. China Chem. 1–33, (2020).

[97]

Senior AW et al. Improved protein structure prediction using potentials from deep learning. Nature, 2020, 577: 706-710

[98]

Elbaz J et al. DNA computing circuits using libraries of DNAzyme subunits. Nat. Nanotechnol., 2010, 5: 417-422

[99]

Chatterjee G, Dalchau N, Muscat RA, Phillips A, Seelig G. A spatially localized architecture for fast and modular DNA computing. Nat. Nanotechnol., 2017, 12: 920-927

[100]

Ketterer P et al. DNA origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex. Nat. Commun., 2018, 9

[101]

Shen Q, Grome MW, Yang Y, Lin C. Engineering lipid membranes with programmable DNA nanostructures. Adv. Biosyst., 2020, 4: 1900215

[102]

Bian X, Zhang Z, Xiong Q, De Camilli P, Lin C. A programmable DNA-origami platform for studying lipid transfer between bilayers. Nat. Chem. Biol., 2019, 15: 830-837

[103]

Zhou K, Zhou Y, Pan V, Wang Q, Ke Y. Programming dynamic assembly of viral proteins with DNA Origami. J. Am. Chem. Soc., 2020, 142: 5929-5932

[104]

Bazak R, Houri M, Achy SE, Hussein W, Refaat T. Passive targeting of nanoparticles to cancer: A comprehensive review of the literature. Mol. Clin. Oncol., 2014, 2: 904-908

[105]

Ma, W. et al. Biomimetic Nanoerythrosome-Coated Aptamer-DNA Tetrahedron/Maytansine Conjugates: pH-responsive and targeted cytotoxicity for HER2-positive breast cancer. Adv Mater. e2109609, (2022).

[106]

Zhang, T., Tian, T. & Lin, Y. Functionalizing framework nucleic acid-based nanostructures for biomedical application. Adv Mater. e2107820, (2021).

[107]

Li J et al. Repair of infected bone defect with clindamycin-tetrahedral DNA nanostructure complex-loaded 3D bioprinted hybrid scaffold. Chem. Eng. J., 2022, 435: 134855

[108]

Erben CM, Goodman RP, Turberfield AJ. Single-molecule protein encapsulation in a rigid DNA cage. Angew. Chem. Int. Ed. Engl., 2006, 45: 7414-7417

[109]

Li S et al. Bioswitchable delivery of microRNA by framework nucleic acids: Application to bone regeneration. Small (Weinh. der Bergstr., Ger.), 2021, 17: e2104359

[110]

Kim KR et al. Shaping rolling circle amplification products into DNA nanoparticles by incorporation of modified nucleotides and their application to in vitro and in vivo delivery of a photosensitizer. Molecules, 2018, 23: 1833

[111]

Miao D, Yu Y, Chen Y, Liu Y, Su G. Facile construction of i-Motif DNA-conjugated gold nanostars as near-infrared and pH dual-responsive targeted drug delivery systems for combined cancer therapy. Mol. Pharm., 2020, 17: 1127-1138

[112]

Liu J et al. A self-assembled DNA nanostructure for targeted and pH-triggered drug delivery to combat doxorubicin resistance. J. Mater. Chem. B, 2016, 4: 3854-3858

[113]

Tian, T. et al. A framework nucleic acid based robotic nanobee for active targeting therapy. Adv. Funct. Mater. 2007342 (2020).

[114]

Xiao D et al. Tetrahedral framework nucleic acids loaded with Aptamer AS1411 for siRNA delivery and gene silencing in malignant melanoma. ACS Appl. Mater. Interfaces, 2021, 13: 6109-6118

[115]

Li, S. et al. Bioswitchable delivery of microRNA by framework nucleic acids: application to bone regeneration. Small. n/a, e2104359, (2021).

[116]

Gačanin J, Synatschke CV, Weil T. Biomedical applications of DNA‐based hydrogels. Adv. Funct. Mater., 2020, 30: 1906253

[117]

Abolhasan R, Mehdizadeh A, Rashidi MR, Aghebati-Maleki L, Yousefi M. Application of hairpin DNA-based biosensors with various signal amplification strategies in clinical diagnosis. Biosens. Bioelectron., 2019, 129: 164-174

[118]

Liu M et al. In vitro selection of a DNA aptamer targeting degraded protein fragments for biosensing. Angew. Chem. Int. Ed. Engl., 2020, 59: 7706-7710

[119]

Pei H et al. A DNA nanostructure-based biomolecular probe carrier platform for electrochemical biosensing. Adv. Mater., 2010, 22: 4754-4758

[120]

Wiraja C et al. Framework nucleic acids as programmable carrier for transdermal drug delivery. Nat. Commun., 2019, 10

[121]

Bi S, Yue S, Zhang S. Hybridization chain reaction: a versatile molecular tool for biosensing, bioimaging, and biomedicine. Chem. Soc. Rev., 2017, 46: 4281-4298

[122]

Tang X et al. Carbon nanotube DNA sensor and sensing mechanism. Nano Lett., 2006, 6: 1632-1636

[123]

Xu H et al. Magnetically assisted DNA assays: High selectivity using conjugated polymers for amplified fluorescent transduction. Nucleic Acids Res, 2005, 33: e83

[124]

Jung C, Allen PB, Ellington AD. A Simple, Cleated DNA Walker That Hangs on to Surfaces. ACS Nano, 2017, 11: 8047-8054

[125]

Zhang, B. et al. Facilitating in situ tumor imaging with a tetrahedral DNA framework‐enhanced hybridization chain reaction probe. Adv. Funct. Mater. 2109728 (2022).

[126]

Jin H et al. Stemmed DNA nanostructure for the selective delivery of therapeutics. Nanoscale, 2018, 10: 7511-7518

[127]

Yang J et al. Self-assembled double-bundle DNA tetrahedron for efficient antisense delivery. ACS Appl. Mater. Interfaces, 2018, 10: 23693-23699

[128]

Xue H et al. DNA tetrahedron-based nanogels for siRNA delivery and gene silencing. Chem. Commun., 2019, 55: 4222-4225

[129]

Zhou, M. et al. A DNA nanostructure-based neuroprotectant against neuronal apoptosis via inhibiting toll-like Receptor 2 signaling pathway in acute ischemic stroke. ACS Nano. https://doi.org/10.1021/acsnano.1c09626 (2021).

[130]

Finke A et al. Functionalized DNA hydrogels produced by polymerase-catalyzed incorporation of non-natural nucleotides as a surface coating for cell culture applications. Adv. Healthc. Mater., 2019, 8: e1900080

[131]

Kim F et al. Functionalized DNA nanostructures as scaffolds for guided mineralization. Chem. Sci., 2019, 10: 10537-10542

[132]

Song Y et al. Discovery of aptamers targeting the receptor-binding domain of the SARS-CoV-2 spike glycoprotein. Anal. Chem., 2020, 92: 9895-9900

[133]

Chen Z, Wu Q, Chen J, Ni X, Dai J. A DNA aptamer based method for detection of SARS-CoV-2 nucleocapsid protein. Virol. Sin., 2020, 35: 351-354

[134]

Wu TH et al. Hybridization chain reactions targeting the severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2). Int. J. Mol. Sci., 2020, 21: 3216

[135]

Wang L et al. Rapid and ultrasensitive electromechanical detection of ions, biomolecules and SARS-CoV-2 RNA in unamplified samples. Nat. Biomed. Eng., 2022, 6: 276-285

[136]

Li F, Li Q, Zuo X, Fan C. DNA framework-engineered electrochemical biosensors. Sci. China Life Sci., 2020, 63: 1130-1141

[137]

Saka SK et al. Immuno-SABER enables highly multiplexed and amplified protein imaging in tissues. Nat. Biotechnol., 2019, 37: 1080-1090

[138]

Wang Z et al. A tubular DNA nanodevice as a siRNA/Chemo-drug co-delivery vehicle for combined cancer therapy. Angew. Chem. Int. Ed. Engl., 2021, 60: 2594-2598

[139]

Qin X et al. Tetrahedral framework nucleic acids-based delivery of microRNA-155 inhibits choroidal neovascularization by regulating the polarization of macrophages. Bioact. Mater., 2021, 14: 134-144

[140]

Jiang D et al. DNA origami nanostructures can exhibit preferential renal uptake and alleviate acute kidney injury. Nat. Biomed. Eng., 2018, 2: 865-877

[141]

Chen Q et al. Sequential therapy of acute kidney injury with a DNA nanodevice. Nano Lett., 2021, 21: 4394-4402

[142]

Zhang Q et al. Tetrahedral framework nucleic acids act as antioxidants in acute kidney injury treatment. Chem. Eng. J., 2021, 413: 127426

[143]

Kim Y, Yin P. Enhancing biocompatible stability of DNA nanostructures using dendritic oligonucleotides and brick motifs. Angew. Chem., 2020, 132: 710-713

[144]

Hahn J, Wickham SF, Shih WM, Perrault SD. Addressing the instability of DNA nanostructures in tissue culture. ACS Nano, 2014, 8: 8765-8775

[145]

Ji X, Zhou Y, Li Q, Song H, Fan C. Protein-mimicking nanoparticles for a cellular regulation of homeostasis. ACS Appl. Mater. Interfaces, 2021, 13: 31331-31336

[146]

Samavedi S, Whittington AR, Goldstein AS. Calcium phosphate ceramics in bone tissue engineering: a review of properties and their influence on cell behavior. Acta biomaterialia, 2013, 9: 8037-8045

[147]

Boshtam M, Asgary S, Kouhpayeh S, Shariati L, Khanahmad H. Aptamers against Pro- and anti-inflammatory cytokines: a Review. Inflammation, 2017, 40: 340-349

[148]

Qin W et al. Bioinspired DNA nanointerface with anisotropic aptamers for accurate capture of circulating tumor cells. Adv. Sci. (Weinh.), 2020, 7: 2000647

[149]

Whitfield CJ et al. Functional DNA–polymer conjugates. Chem. Rev., 2021, 121: 11030-11084

[150]

Liu X et al. Complex silica composite nanomaterials templated with DNA origami. Nature, 2018, 559: 593-598

[151]

Zhang Z-L, Wu Y-Y, Xi K, Sang J-P, Tan Z-J. Divalent ion-mediated DNA-DNA interactions: a comparative study of triplex and duplex. Biophysical J., 2017, 113: 517-528

[152]

Yao C et al. Double rolling circle amplification generates physically cross-linked DNA network for stem cell fishing. J. Am. Chem. Soc., 2020, 142: 3422-3429

AI Summary AI Mindmap
PDF

147

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/