DNA nanofabrication by scanning near-field photolithography of oligo (ethylene glycol) terminated SAMs: Controlled scan-rate dependent switching between head group oxidation and tail group degradation
Sun, Shuqing and Thompson, David G. and Graham, Duncan and Leggett, Graham J. (2011) DNA nanofabrication by scanning near-field photolithography of oligo (ethylene glycol) terminated SAMs: Controlled scan-rate dependent switching between head group oxidation and tail group degradation. Journal of Materials Chemistry, 21 (37). pp. 14173-14177. ISSN 0959-9428 (https://doi.org/10.1039/c1jm11803j)
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The use of scanning near-field photolithography (SNP) to fabricate DNA nanostructures is described. Two different strategies were employed to generate nanoscale features in oligo(ethylene glycol) (OEG) terminated alkylthiolate self-assembled monolayers (SAMs) on gold. At long exposure times, complete photooxidation of the SAM molecules enabled their displacement by amino-terminated thiol molecules, which were subsequently used to attach ss-DNA molecules; while short exposure times resulted in partial photochemical conversion of the terminal OEG group of the adsorbate to an aldehyde group facilitating the direct attachment of amino-DNA molecules. Arrays of DNA functionalized metal-nanoparticles were then assembled onto the ss-DNA patches through specific DNA hybridization. This methodology provides a facile approach for the assembly of bio-functionalised nanoparticles onto nanofeatures embedded in an inert background and will prove useful in biosensing applications.
ORCID iDs
Sun, Shuqing, Thompson, David G., Graham, Duncan ORCID: https://orcid.org/0000-0002-6079-2105 and Leggett, Graham J.;-
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Item type: Article ID code: 33593 Dates: DateEvent2011PublishedSubjects: Science > Chemistry > Physical and theoretical chemistry Department: Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > BionanotechnologyDepositing user: Pure Administrator Date deposited: 17 Oct 2011 10:17 Last modified: 11 Nov 2024 09:50 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/33593