Abstract
Carbon monoxide (CO) is an emerging gasotransmitter and reactive carbon species with broad anti-inflammatory,
cytoprotective, and neurotransmitter functions along with therapeutic potential for the treatment of cardiovascular diseases.
The study of CO chemistry in biology and medicine relative to other prominent gasotransmitters such as NO and H2S
remains challenging, in large part due to limitations in available tools for the direct visualization of this transient and freely
diffusing small molecule in complex living systems. Here we report a ligand-directed activity-based sensing (ABS) approach
to CO detection through palladium-mediated carbonylation chemistry. Specifically, the design and synthesis of a series of
ABS probes with systematic alterations in the palladium-ligand environment (e.g., sp3-S, sp3-N, sp2-N) establish structureactivity relationships for palladacycles to confer selective reactivity with CO under physiological conditions. These
fundamental studies led to the development of an optimized probe, termed Carbon Monoxide Probe-3 Ester Pyridine (COP3E-Py), which enables imaging of CO release in live cell and brain settings, including monitoring of endogenous CO
production that triggers presynaptic dopamine release in fly brains. This work provides a unique tool for studying CO in
living systems and establishes the utility of a synthetic methods approach to activity-based sensing using principles of
organometallic chemistry
Supplementary materials
Title
CJC COP CO Probes SI
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Title
COP-1-PY
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Title
COP-1
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Title
COP-1'
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