Programmable Photoluminescence via Intrinsic and DNA-Fluorophore Association in a Mixed Cluster Heterometallic MOF.
Dorina F Sava GallisKimberly S ButlerCharles J PearceNichole ValdezMark A RodriguezPublished in: ACS applied materials & interfaces (2022)
A rapid and facile design strategy to create a highly complex optical tag with programmable, multimodal photoluminescent properties is described. This was achieved via intrinsic and DNA-fluorophore hidden signatures. As a first covert feature of the tag, an intricate novel heterometallic near-infrared (NIR)-emitting mesoporous metal-organic framework (MOF) was designed and synthesized. The material is constructed from two chemically distinct, homometallic hexanuclear clusters based on Nd and Yb. Uniquely, the Nd-based cluster is observed here for the first time in a MOF and consists of two staggered Nd μ 3 -oxo trimers. To generate controlled, multimodal, and tailorable emission with difficult to counterfeit features, the NIR-emissive MOF was post-synthetically modified via a fluorescent DNA oligo labeling design strategy. The surface attachment of several distinct fluorophores, including the simultaneous attachment of up to three distinct fluorescently labeled oligos was achieved, with excitation and emission properties across the visible spectrum (480-800 nm). The DNA inclusion as a secondary covert element in the tag was demonstrated via the detection of SYBR Gold dye association. Importantly, the approach implemented here serves as a rapid and tailorable way to encrypt distinct information in a facile and modular fashion and provides an innovative technology in the quest toward complex optical tags.
Keyphrases
- metal organic framework
- circulating tumor
- fluorescent probe
- quantum dots
- cell free
- single molecule
- living cells
- loop mediated isothermal amplification
- photodynamic therapy
- energy transfer
- high resolution
- nucleic acid
- high speed
- drug release
- circulating tumor cells
- healthcare
- deep learning
- label free
- dna methylation
- chronic pain
- gene expression
- social media
- reduced graphene oxide
- mass spectrometry