Phosphatase-inert glucosamine 6-phosphate mimics serve as actuators of the glms riboswitch

Xiang Fei, Thomas Holmes, Julianna Diddle, Lauren Hintz, Dan Delaney, Alex Stock, Danielle Renner, Molly McDevitt, David B. Berkowitz, Juliane K. Strauss-Soukup

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

The glmS riboswitch is unique among gene-regulating riboswitches and catalytic RNAs. This is because its own metabolite, glucosamine-6-phosphate (GlcN6P), binds to the riboswitch and catalytically participates in the RNA self-cleavage reaction, thereby providing a novel negative feedback mechanism. Given that a number of pathogens harbor the glmS riboswitch, artificial actuators of this potential RNA target are of great interest. Structural/kinetic studies point to the 2-amino and 6-phosphate ester functionalities in GlcN6P as being crucial for this actuation. As a first step toward developing artificial actuators, we have synthesized a series of nine GlcN6P analogs bearing phosphatase-inert surrogates in place of the natural phosphate ester. Self-cleavage assays with the Bacillus cereus glmS riboswitch give a broad SAR. Two analogs display significant activity, namely, the 6-deoxy-6-phosphonomethyl analog (5) and the 6-O-malonyl ether (13). Kinetic profiles show a 22-fold and a 27-fold higher catalytic efficiency, respectively, for these analogs vs glucosamine (GlcN). Given their nonhydrolyzable phosphate surrogate functionalities, these analogs are arguably the most robust artificial glmS riboswitch actuators yet reported. Interestingly, the malonyl ether (13, extra O atom) is much more effective than the simple malonate (17), and the "sterically true" phosphonate (5) is far superior to the chain-truncated (7) or chain-extended (11) analogs, suggesting that positioning via Mg coordination is important for activity. Docking results are consistent with this view. Indeed, the viability of the phosphonate and 6-O-malonyl ether mimics of GlcN6P points to a potential new strategy for artificial actuation of the glmS riboswitch in a biological setting, wherein phosphatase-resistance is paramount.

Original languageEnglish
Pages (from-to)2875-2882
Number of pages8
JournalACS Chemical Biology
Volume9
Issue number12
DOIs
StatePublished - Dec 19 2014

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Riboswitch
Phosphoric Monoester Hydrolases
Actuators
Ether
Organophosphonates
Phosphates
Esters
Bearings (structural)
RNA Cleavage
RNA
Bacillus cereus
Catalytic RNA
Kinetics
Glucosamine
Pathogens
Metabolites
Ports and harbors
glucosamine 6-phosphate
Assays
Genes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Medicine
  • Medicine(all)

Cite this

Phosphatase-inert glucosamine 6-phosphate mimics serve as actuators of the glms riboswitch. / Fei, Xiang; Holmes, Thomas; Diddle, Julianna; Hintz, Lauren; Delaney, Dan; Stock, Alex; Renner, Danielle; McDevitt, Molly; Berkowitz, David B.; Strauss-Soukup, Juliane K.

In: ACS Chemical Biology, Vol. 9, No. 12, 19.12.2014, p. 2875-2882.

Research output: Contribution to journalArticle

Fei, X, Holmes, T, Diddle, J, Hintz, L, Delaney, D, Stock, A, Renner, D, McDevitt, M, Berkowitz, DB & Strauss-Soukup, JK 2014, 'Phosphatase-inert glucosamine 6-phosphate mimics serve as actuators of the glms riboswitch', ACS Chemical Biology, vol. 9, no. 12, pp. 2875-2882. https://doi.org/10.1021/cb500458f
Fei, Xiang ; Holmes, Thomas ; Diddle, Julianna ; Hintz, Lauren ; Delaney, Dan ; Stock, Alex ; Renner, Danielle ; McDevitt, Molly ; Berkowitz, David B. ; Strauss-Soukup, Juliane K. / Phosphatase-inert glucosamine 6-phosphate mimics serve as actuators of the glms riboswitch. In: ACS Chemical Biology. 2014 ; Vol. 9, No. 12. pp. 2875-2882.
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