2015
DOI: 10.1039/c4cc09516b
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A near-infrared light-controlled system for reversible presentation of bioactive ligands using polypeptide-engineered functionalized gold nanorods

Abstract: A near-infrared light-controlled hybrid platform with polypeptide-engineered functionalized gold nanorods has been designed for reversible presentation of the immobilized ligands to cell surface receptors on the engineered materials.

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Cited by 20 publications
(27 citation statements)
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“…The constant immobilization of the RGD prevents unintended side effects from soluble RGD in the media and allows for multiple cycles of screening with PEG. This strategy has been further explored to incorporate a near-IR phototrigger to release the PEG molecules, thereby increasing spatiotemporal control 67 . In another example, a hydrogel was engineered to reversibly expose cell adhesion sites by folding and unfolding in response to aptamer hybridization 65 (FIG.…”
Section: Exchangeable Ligand Presentationmentioning
confidence: 99%
“…The constant immobilization of the RGD prevents unintended side effects from soluble RGD in the media and allows for multiple cycles of screening with PEG. This strategy has been further explored to incorporate a near-IR phototrigger to release the PEG molecules, thereby increasing spatiotemporal control 67 . In another example, a hydrogel was engineered to reversibly expose cell adhesion sites by folding and unfolding in response to aptamer hybridization 65 (FIG.…”
Section: Exchangeable Ligand Presentationmentioning
confidence: 99%
“…Multiple photothermal agents have been successful developed, such as melanin [10], indocyanine green [11], carbon nanotubes [12] and gold nanomaterials [13]. Particularly, gold nanorods (GNR) -based nanoparticles have been extensively investigated in biomedicine due to their unique shape effects [8,14,15]. GNR can produce stable photoacoustic signals that make them trackable in vivo.…”
Section: Introductionmentioning
confidence: 99%
“…[52] Fluorescencei mages of cells adsorbed on LbL PTAPE films are shown in Figure 6a.B efore UV irradiation, the densities of adhered cellsa re 3218 AE 390 (Figure 6a1), 14909 AE 1654 (Figure 6a2), 16909 AE 2363 (Figure 6a3), and 16045 AE 927 cm À2 (Figure 6a4) on the flat and rough substrates with pillar spacingso f5 ,1 0a nd 20 mm, respectively.I ti sk nownt hat more cells can be adhered to hydrophobic surfaces than to hydrophilic surfaces. [4][5][6][7][8][9][10][11][12] The trans-azobenzene films are relatively hydrophobic, to which more cells can adhere (Figure 6a1-a4). After UV irradiation, azobenzene chromophores become cis in configuration, and have higherd ipole moments and surface free energies, and the resulting surfaces exhibit am uch lower adhesion capacity (Figure 6a5-a8).…”
Section: Resultsmentioning
confidence: 99%
“…[1][2][3] Understanding the adhesion of cells to substrates is not only helpful for preparingf unctional coatings of medical implants,b ut also significant for establishing an ext generation of interface materials, integratingc ancerc ellsi nto specific surfaces and achieving highly sensitive biosensing. In recent years, various strategies involving stimuli such as changes in pH, [4,5] temperature, [6] voltage, [7,8] and light [9][10][11][12] have been developed as triggersf or controlling cell adhesion on the surfaces. Amongt hese, the light-stimulus response system has promising potential because of its precise spatiotemporal control and convenient operation.…”
Section: Introductionmentioning
confidence: 99%