10th anniversary of discovering cGAMP: synthesis and beyond

被引:3
|
作者
Chen, Chuo [1 ]
机构
[1] UT Southwestern Med Ctr, Dept Biochem, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
关键词
C-DI-GMP; SOLID-PHASE SYNTHESIS; HIGH-YIELD PROTECTION; STEREOSELECTIVE-SYNTHESIS; STEREOCONTROLLED SYNTHESIS; CYCLIC DINUCLEOTIDE; CHEMICAL-SYNTHESIS; ADAPTER PROTEIN; DITHYMIDINE PHOSPHOROTHIOATES; PURINE RIBONUCLEOSIDES;
D O I
10.1039/d2qo02033e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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.
引用
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页码:1086 / 1098
页数:13
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