2019
DOI: 10.1021/acsnano.8b06170
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Multivalent Traptavidin–DNA Conjugates for the Programmable Assembly of Nanostructures

Abstract: Here, we explore the extended utility of two important functional biomolecules, DNA and protein, by hybridizing them through avidin–biotin conjugation. We report a simple yet scalable technique of successive magnetic separations to synthesize traptavidin–DNA conjugates with four distinct DNA binding sites that can be used as a supramolecular building block for programmable assembly of nanostructures. Using this nanoassembly platform, we fabricate several different plasmonic nanostructures with various metallic… Show more

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Cited by 23 publications
(18 citation statements)
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References 61 publications
(80 reference statements)
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“…Traptavidin is a recently reported mutant of streptavidin with a lower koff rate for biotin binding versus streptavidin [13]. These mutations effectively increase the overall residence time of the complex with biotin, making Traptavidin a potentially more attractive alternative to streptavidin for biomaterials applications [20]. To test this, we constructed an expression cassette for an MPB-TEVS219V-TRPT fusion protein, expressing and immobilizing this protein fusion as previously described.…”
Section: Resultsmentioning
confidence: 99%
“…Traptavidin is a recently reported mutant of streptavidin with a lower koff rate for biotin binding versus streptavidin [13]. These mutations effectively increase the overall residence time of the complex with biotin, making Traptavidin a potentially more attractive alternative to streptavidin for biomaterials applications [20]. To test this, we constructed an expression cassette for an MPB-TEVS219V-TRPT fusion protein, expressing and immobilizing this protein fusion as previously described.…”
Section: Resultsmentioning
confidence: 99%
“…Compared with QD assemblies, NP-QD heterostructures were easily purified and concentrated by centrifugation and magnetic separation. [16,34,51] Plasmonic metal NPs and semiconductor heterostructures were obtained by optimizing the DNA sequences and concentrations on each NP. For example, by controlling the DNA density to ≈0.28 DNA per nm 2 on Au NPs, about six or seven QDs were assembled on every Au NP (Figure 3a).…”
Section: Plasmonic Metal Nps and Semiconductor Heterostructuresmentioning
confidence: 99%
“…DNA molecules contain abundant functional groups and unique biometric recognition capabilities, which allow for the precise modification and programmable construction of NP assemblies. [ 16–18 ] DNA can be self‐assembled into desired 3D shapes, [ 19 ] and the configuration of plasmonic heterogeneous nanoassemblies can be controlled by adjusting the sequence, length, and configuration of DNA. [ 20 ] Oriented self‐assembly holds great promise for controlling the morphologies of nanostructures beyond what is possible using conventional systems.…”
Section: Introductionmentioning
confidence: 99%
“…Techniques using nanochannels, 15-17 magnetic nanobeads, 18,19 evaporation 20 and Langmuir-54 Blodgett films 21 have been explored to concentrate and deposit suspended particles to surfaces, but depositing them precisely to designated locations, which is important for applications like multiplexing sensors, are still challenging. Previous studies show that fluid flow around an photothermally generated surface bubble can be a promising deposition methods with precision.…”
Section: Introductionmentioning
confidence: 99%