Bio-orthogonal Supramolecular Latching inside Live Animals and Its Application for in Vivo Cancer Imaging.
Meng LiSungwan KimAra LeeAnnadka ShrinidhiYoung Ho KoHae Gyun LimHyung Ham KimKi Beom BaeKyeng Min ParkKimoon KimPublished in: ACS applied materials & interfaces (2019)
Here, we demonstrate a supramolecular latching tool for bio-orthogonal noncovalent anchoring of small synthetic molecules in live animal models using a fully synthetic high-affinity binding pair between cucurbit[7]uril (CB[7]) and adamantylammonium (AdA). This supramolecular latching system is small (∼1 kDa), ensuring efficient uptake into cells, tissues, and whole organisms. It is also chemically robust and resistant to enzymatic degradation and analogous to well-characterized biological systems in terms of noncovalent binding. Occurrence of fluorescence resonance energy transfer (FRET) between cyanine 3-CB[7] (Cy3-CB[7]) and boron-dipyrromethene 630/650X-AdA (BDP630/650-AdA) inside a live worm (Caenorhabditis elegans) indicates efficient in situ high-affinity association between AdA and CB[7] inside live animals. In addition, selective visualization of a cancer site of a live mouse upon supramolecular latching of cyanine 5-AdA (Cy5-AdA) on prelocalized CB[7]-conjugating antibody on the cancer site demonstrates the potential of this synthetic system for in vivo cancer imaging. These findings provide a fresh insight into the development of new chemical biology tools and medical therapeutic systems.
Keyphrases
- energy transfer
- papillary thyroid
- squamous cell
- quantum dots
- healthcare
- gene expression
- squamous cell carcinoma
- mass spectrometry
- single molecule
- lymph node metastasis
- water soluble
- nitric oxide
- multidrug resistant
- signaling pathway
- induced apoptosis
- cell death
- oxidative stress
- gram negative
- childhood cancer
- risk assessment
- cell cycle arrest
- living cells