10th anniversary of discovering cGAMP: synthesis and beyond.
Chuo ChenPublished in: Organic chemistry frontiers : an international journal of organic chemistry (2023)
The discovery of cGAMP in 2012 filled an important gap in our understanding of innate immune signaling. It has been known for over a century that DNA can induce immune responses, but the underlying mechanism was not clear. With the identification of STING as a key player in interferon induction, the DNA detector that activates STING was the last missing link in TBK1-IRF3 signaling. Somewhat unexpectedly, it turns out that nature relays the DNA danger signal through a small molecule. cGAMP is a cyclic dinucleotide produced from cyclodimerization of ATP and GTP upon detection of cytosolic DNA by cGAS, a previously uncharacterized protein, to promote the assembly of the STING signalosome. This article covers a personal account of the discovery of cGAMP, a short history of the relevant nucleotide chemistry, and a summary of the latest development in this field of research in chemistry. It is the author's hope that, with a historic perspective, the readers can better appreciate the synergy between chemistry and biology in drug development.
Keyphrases
- small molecule
- circulating tumor
- cell free
- single molecule
- immune response
- dendritic cells
- protein protein
- innate immune
- nucleic acid
- drug discovery
- high throughput
- toll like receptor
- computed tomography
- quantum dots
- magnetic resonance imaging
- single cell
- loop mediated isothermal amplification
- bioinformatics analysis
- label free