Chemiluminescence
probes are considered to be among the most sensitive
diagnostic tools that provide high signal-to-noise ratio for various
applications such as DNA detection and immunoassays. We have developed
a new molecular methodology to design and foresee light-emission properties
of turn-ON chemiluminescence dioxetane probes suitable for use under
physiological conditions. The methodology is based on incorporation
of a substituent on the benzoate species obtained during the chemiexcitation
pathway of Schaap’s adamantylidene–dioxetane probe.
The substituent effect was initially evaluated on the fluorescence
emission generated by the benzoate species and then on the chemiluminescence
of the dioxetane luminophores. A striking substituent effect on the
chemiluminescence efficiency of the probes was obtained when acrylate
and acrylonitrile electron-withdrawing groups were installed. The
chemiluminescence quantum yield of the best probe was more than 3
orders of magnitude higher than that of a standard, commercially available
adamantylidene–dioxetane probe. These are the most powerful
chemiluminescence dioxetane probes synthesized to date that are suitable
for use under aqueous conditions. One of our probes was capable of
providing high-quality chemiluminescence cell images based on endogenous
activity of β-galactosidase. This is the first demonstration
of cell imaging achieved by a non-luciferin small-molecule probe with
direct chemiluminescence mode of emission. We anticipate that the
strategy presented here will lead to development of efficient chemiluminescence
probes for various applications in the field of sensing and imaging.
Natural killer (NK) cells are immune cells that can kill certain types of cancer cells. Adoptive transfer of NK cells represents a promising immunotherapy for malignant tumours; however, there is a lack of methods to validate anti‐tumour activity of NK cells in vivo. Herein, we report a new chemiluminescent probe to image in situ the granzyme B‐mediated killing activity of NK cells against cancer cells. We have optimised a granzyme B‐specific construct using an activatable phenoxydioxetane reporter so that enzymatic cleavage of the probe results in bright chemiluminescence. The probe shows high selectivity for active granzyme B over other proteases and higher signal‐to‐noise ratios than commercial fluorophores. Finally, we demonstrate that the probe can detect NK cell activity in mouse models, being the first chemiluminescent probe for in vivo imaging of NK cell activity in live tumours.
The prostate specific antigen (PSA), a serine protease with chymotrypsin-like activity, is predominantly expressed in the prostate and is considered as the most common marker in use to identify and follow the progress of prostate cancer. In addition, it is also now accepted as a marker for detecting semen in criminal cases. Here, we describe the design, synthesis, and evaluation of the first chemiluminescence probe for detection of PSA enzymatic activity. The probe activation mechanism is based on a catalytic cleavage of a specific peptidyl substrate, followed by a release of a phenoxy-dioxetane luminophore, that then undergoes efficient chemiexcitation to emit a green photon. The probe exhibits a significant turn-on response upon reaction with PSA and produces strong light emission signal with an extremely high signal-to-noise ratio. Comparison of the chemiluminescence probe with an analogous fluorescence probe showed superior detection capability in terms of response time and sensitivity. In addition, the probe was able to efficiently detect and image human semen traces on fabric, even after 3 days from sample preparation. The advantageous sensitivity and simplicity of a chemiluminescence assay to detect seminal fluid was effectively demonstrated by on-site measurements using a small portable luminometer. It is expected that the new chemiluminescence probe would be broadly useful for numerous applications in which PSA detection or imaging is required.
Adamantyl‐dioxetane luminophores are an important class of chemiluminescent molecular probes for diagnostics and imaging. We have developed a new efficient synthetic route for preparation of adamantyl‐enolether as precursors for dioxetane chemiluminescent luminophores. The synthesis is convergent, using an unusual Stille cross‐coupling reaction employing a stannane‐enolether, to directly afford adamantyl‐enolether. In a following simple step, the dioxetane is obtained by oxidation of the enolether precursor with singlet‐oxygen. The scope of this synthetic route is broad since a large number of haloaryl substrates are either commercially available or easily accessible. Such a late‐stage derivatization strategy simplifies the rapid exploration of novel luminogenic molecular structures in a library format and simplifies the synthesis of known dioxetane luminophores. We expect that this new synthetic strategy will be particularly useful in the design and synthesis of yet unexplored dioxetane chemiluminescent luminophores.
Influenza A virus is the most virulent influenza subtype and is associated with large-scale global pandemics characterized by high levels of morbidity and mortality. Developing simple and sensitive molecular methods...
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