TY - JOUR
T1 - Synthetic ligands for PreQ 1 riboswitches provide structural and mechanistic insights into targeting RNA tertiary structure
AU - Connelly, Colleen M.
AU - Numata, Tomoyuki
AU - Boer, Robert E.
AU - Moon, Michelle H.
AU - Sinniah, Ranu S.
AU - Barchi, Joseph J.
AU - Ferré-D’Amaré, Adrian R.
AU - Schneekloth, John S.
N1 - Funding Information:
We thank the staff of beamlines 5.0.1 and 5.0.2 of the ALS for diffraction data collection, and S. Bachas, C. Jones, and R. Trachman III for discussions. We thank J. Kelley for assistance with HRMS work. This work was supported in part the by the Center for Cancer Research of the National Cancer Institute, NIH (1 ZIA BC011585 04), the Intramural Program of the National Heart, Lung and Blood Institute, NIH, the Japan Society for the Promotion of Science (JSPS KAKENHI Grant Number 16KK0166), and a grant from the Astellas Foundation for Research on Metabolic Disorders.
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Riboswitches are naturally occurring RNA aptamers that regulate gene expression by binding to specific small molecules. Riboswitches control the expression of essential bacterial genes and are important models for RNA-small molecule recognition. Here, we report the discovery of a class of synthetic small molecules that bind to PreQ 1 riboswitch aptamers. These molecules bind specifically and reversibly to the aptamers with high affinity and induce a conformational change. Furthermore, the ligands modulate riboswitch activity through transcriptional termination despite no obvious chemical similarity to the cognate ligand. X-ray crystallographic studies reveal that the ligands share a binding site with the cognate ligand but make different contacts. Finally, alteration of the chemical structure of the ligand causes changes in the mode of RNA binding and affects regulatory function. Thus, target- and structure-based approaches can be used to identify and understand the mechanism of synthetic ligands that bind to and regulate complex, folded RNAs.
AB - Riboswitches are naturally occurring RNA aptamers that regulate gene expression by binding to specific small molecules. Riboswitches control the expression of essential bacterial genes and are important models for RNA-small molecule recognition. Here, we report the discovery of a class of synthetic small molecules that bind to PreQ 1 riboswitch aptamers. These molecules bind specifically and reversibly to the aptamers with high affinity and induce a conformational change. Furthermore, the ligands modulate riboswitch activity through transcriptional termination despite no obvious chemical similarity to the cognate ligand. X-ray crystallographic studies reveal that the ligands share a binding site with the cognate ligand but make different contacts. Finally, alteration of the chemical structure of the ligand causes changes in the mode of RNA binding and affects regulatory function. Thus, target- and structure-based approaches can be used to identify and understand the mechanism of synthetic ligands that bind to and regulate complex, folded RNAs.
UR - http://www.scopus.com/inward/record.url?scp=85063737427&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85063737427&partnerID=8YFLogxK
U2 - 10.1038/s41467-019-09493-3
DO - 10.1038/s41467-019-09493-3
M3 - Article
C2 - 30940810
AN - SCOPUS:85063737427
VL - 10
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
IS - 1
M1 - 1501
ER -