Recognition of cyclic dinucleotides and folates by human SLC19A1

Qixiang Zhang, Xuyuan Zhang, Yalan Zhu, Panpan Sun, Liwei Zhang, Junxiao Ma, Yong Zhang, Lingan Zeng, Xiaohua Nie, Yina Gao, Zhaolong Li, Songqing Liu, Jizhong Lou, Ang Gao (), Liguo Zhang () and Pu Gao ()
Additional contact information
Qixiang Zhang: Chinese Academy of Sciences
Xuyuan Zhang: Chinese Academy of Sciences
Yalan Zhu: Beijing Institute of Technology
Panpan Sun: Chinese Academy of Sciences
Liwei Zhang: Chinese Academy of Sciences
Junxiao Ma: Chinese Academy of Sciences
Yong Zhang: Chinese Academy of Sciences
Lingan Zeng: Chinese Academy of Sciences
Xiaohua Nie: Chinese Academy of Sciences
Yina Gao: Chinese Academy of Sciences
Zhaolong Li: Chinese Academy of Sciences
Songqing Liu: Chinese Academy of Sciences
Jizhong Lou: University of Chinese Academy of Sciences
Ang Gao: Beijing Institute of Technology
Liguo Zhang: Chinese Academy of Sciences
Pu Gao: Chinese Academy of Sciences

Nature, 2022, vol. 612, issue 7938, 170-176

Abstract: Abstract Cyclic dinucleotides (CDNs) are ubiquitous signalling molecules in all domains of life1,2. Mammalian cells produce one CDN, 2′3′-cGAMP, through cyclic GMP–AMP synthase after detecting cytosolic DNA signals3–7. 2′3′-cGAMP, as well as bacterial and synthetic CDN analogues, can act as second messengers to activate stimulator of interferon genes (STING) and elicit broad downstream responses8–21. Extracellular CDNs must traverse the cell membrane to activate STING, a process that is dependent on the solute carrier SLC19A122,23. Moreover, SLC19A1 represents the major transporter for folate nutrients and antifolate therapeutics24,25, thereby placing SLC19A1 as a key factor in multiple physiological and pathological processes. How SLC19A1 recognizes and transports CDNs, folate and antifolate is unclear. Here we report cryo-electron microscopy structures of human SLC19A1 (hSLC19A1) in a substrate-free state and in complexes with multiple CDNs from different sources, a predominant natural folate and a new-generation antifolate drug. The structural and mutagenesis results demonstrate that hSLC19A1 uses unique yet divergent mechanisms to recognize CDN- and folate-type substrates. Two CDN molecules bind within the hSLC19A1 cavity as a compact dual-molecule unit, whereas folate and antifolate bind as a monomer and occupy a distinct pocket of the cavity. Moreover, the structures enable accurate mapping and potential mechanistic interpretation of hSLC19A1 with loss-of-activity and disease-related mutations. Our research provides a framework for understanding the mechanism of SLC19-family transporters and is a foundation for the development of potential therapeutics.

Date: 2022
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DOI: 10.1038/s41586-022-05452-z

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