4.7 Article

Graphene Quantum Dot Oxidation Governs Noncovalent Biopolymer Adsorption

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SCIENTIFIC REPORTS
卷 10, 期 1, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41598-020-63769-z

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资金

  1. NIH NIDA CEBRA award [R21DA044010]
  2. Burroughs Wellcome Fund Career Award at the Scientific Interface (CASI)
  3. Simons Foundation
  4. Stanley Fahn PDF Junior Faculty Grant [PF-JFA-1760]
  5. Beckman Foundation Young Investigator Award
  6. Moore Foundation award
  7. USDA NIFA grant
  8. NSF/USDA BBT EAGER grant
  9. DARPA Young Investigator Award
  10. NSF Graduate Research Fellowship [NSF DGE 1752814]
  11. NIH [S10OD023532]

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Graphene quantum dots (GQDs) are an allotrope of carbon with a planar surface amenable to functionalization and nanoscale dimensions that confer photoluminescence. Collectively, these properties render GQDs an advantageous platform for nanobiotechnology applications, including optical biosensing and delivery. Towards this end, noncovalent functionalization offers a route to reversibly modify and preserve the pristine GQD substrate, however, a clear paradigm has yet to be realized. Herein, we demonstrate the feasibility of noncovalent polymer adsorption to GQD surfaces, with a specific focus on single-stranded DNA (ssDNA). We study how GQD oxidation level affects the propensity for polymer adsorption by synthesizing and characterizing four types of GQD substrates ranging 60-fold in oxidation level, then investigating noncovalent polymer association to these substrates. Adsorption of ssDNA quenches intrinsic GQD fluorescence by 31.5% for low-oxidation GQDs and enables aqueous dispersion of otherwise insoluble no-oxidation GQDs. ssDNA-GQD complexation is confirmed by atomic force microscopy, by inducing ssDNA desorption, and with molecular dynamics simulations. ssDNA is determined to adsorb strongly to no-oxidation GQDs, weakly to low-oxidation GQDs, and not at all for heavily oxidized GQDs. Finally, we reveal the generality of the adsorption platform and assess how the GQD system is tunable by modifying polymer sequence and type.

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