The Mechanisms of RNA SHAPE Chemistry

• Published in: Journal of the American Chemical Society 2012-04, Vol.134 (15), p.6617-6624
• Main Authors: McGinnis, Jennifer L., Dunkle, Jack A., Cate, Jamie H. D., Weeks, Kevin M.
• Format: Article
• Language: English
• Subjects: Acylation; Hydroxyl Radical; Nucleic Acid Conformation; RNA - chemistry; RNA, Ribosomal - chemistry
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja2104075

The biological functions of RNA are ultimately governed by the local environment at each nucleotide. Selective 2′-hydroxyl acylation analyzed by primer extension (SHAPE) chemistry is a powerful approach for measuring nucleotide structure and dynamics in diverse biological environments. SHAPE reagents acylate the 2′-hydroxyl group at flexible nucleotides because unconstrained nucleotides preferentially sample rare conformations that enhance the nucleophilicity of the 2′-hydroxyl. The critical corollary is that some constrained nucleotides must be poised for efficient reaction at the 2′-hydroxyl group. To identify such nucleotides, we performed SHAPE on intact crystals of the Escherichia coli ribosome, monitored the reactivity of 1490 nucleotides in 16S rRNA, and examined those nucleotides that were hyper-reactive toward SHAPE and had well-defined crystallographic conformations. Analysis of these conformations revealed that 2′-hydroxyl reactivity is broadly facilitated by general base catalysis involving multiple RNA functional groups and by two specific orientations of the bridging 3′-phosphate group. Nucleotide analog studies confirmed the contributions of these mechanisms to SHAPE reactivity. These results provide a strong mechanistic explanation for the relationship between SHAPE reactivity and local RNA dynamics and will facilitate interpretation of SHAPE information in the many technologies that make use of this chemistry.