Programming nanoparticle valence bonds with single-stranded DNA encoders
文献类型:期刊论文
作者 | Yao, GB; Li, J; Li, Q; Chen, XL; Liu, XG; Wang, F; Qu, ZB; Ge, ZL; Narayanan, RP; Williams, D |
刊名 | NATURE MATERIALS |
出版日期 | 2019 |
页码 | - |
ISSN号 | 1476-1122 |
关键词 | PLASMONIC NANOSTRUCTURES ASYMMETRIC FUNCTIONALIZATION GOLD NANOPARTICLES PATCHY PARTICLES QUANTUM DOTS FORCE-FIELDS OLIGONUCLEOTIDE SUPERLATTICES |
DOI | 10.1038/s41563-019-0549-3 |
文献子类 | 期刊论文 |
英文摘要 | Nature has evolved strategies to encode information within a single biopolymer to program biomolecular interactions with characteristic stoichiometry, orthogonality and reconfigurability. Nevertheless, synthetic approaches for programming molecular reactions or assembly generally rely on the use of multiple polymer chains (for example, patchy particles). Here we demonstrate a method for patterning colloidal gold nanoparticles with valence bond analogues using single-stranded DNA encoders containing polyadenine (polyA). By programming the order, length and sequence of each encoder with alternating polyA/non-polyA domains, we synthesize programmable atom-like nanoparticles (PANs) with n-valence that can be used to assemble a spectrum of low-coordination colloidal molecules with different composition, size, chirality and linearity. Moreover, by exploiting the reconfigurability of PANs, we demonstrate dynamic colloidal bond-breaking and bond-formation reactions, structural rearrangement and even the implementation of Boolean logic operations. This approach may be useful for generating responsive functional materials for distinct technological applications. Single-stranded DNA encoders containing polyadenine domains endow colloidal gold nanoparticles with programmable bond valence, orthogonality and reconfigurability, thus achieving post-synthetic control over colloidal structures. |
语种 | 英语 |
源URL | [http://ir.sinap.ac.cn/handle/331007/32172] |
专题 | 上海应用物理研究所_中科院上海应用物理研究所2011-2017年 |
作者单位 | 1.Univ Groningen, Stratingh Inst Chem, Groningen, Netherlands; 2.Shanghai Jiao Tong Univ, Renji Hosp, Frontiers Sci Ctr Transformat Mol, Sch Chem & Chem Engn,Inst Mol Med,Sch Med, Shanghai, Peoples R China; 3.Chinese Acad Sci, Shanghai Inst Appl Phys, Div Phys Biol, CAS Key Lab Interfacial Phys & Technol, Shanghai, Peoples R China; 4.Chinese Acad Sci, Shanghai Adv Res Inst, Zhangjiang Lab, Shanghai Synchrotron Radiat Facil, Shanghai, Peoples R China; 5.Arizona State Univ, Ctr Mol Design & Biomimet, Biodesign Inst, Sch Mol Sci, Tempe, AZ USA; 6.Arizona State Univ, Erying Mat Ctr, Off Knowledge Enterprise Dev, Tempe, AZ USA; 7.East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai, Peoples R China; 8.East China Univ Sci & Technol, Feringa Nobel Prize Scientist Joint Res Ctr, Sch Chem & Mol Engn, Shanghai, Peoples R China |
推荐引用方式 GB/T 7714 | Yao, GB,Li, J,Li, Q,et al. Programming nanoparticle valence bonds with single-stranded DNA encoders[J]. NATURE MATERIALS,2019:-. |
APA | Yao, GB.,Li, J.,Li, Q.,Chen, XL.,Liu, XG.,...&Fan, CH.(2019).Programming nanoparticle valence bonds with single-stranded DNA encoders.NATURE MATERIALS,-. |
MLA | Yao, GB,et al."Programming nanoparticle valence bonds with single-stranded DNA encoders".NATURE MATERIALS (2019):-. |
入库方式: OAI收割
来源:上海应用物理研究所
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