Abstract

X-ray crystallography remains a powerful method to gain atomistic insights into the catalytic and regulatory functions of RNA molecules. However, the technique requires the preparation of diffraction-quality crystals. This is often a resource- and time-consuming venture because RNA crystallization is hindered by the conformational heterogeneity of RNA, as well as the limited opportunities for stereospecific intermolecular interactions between RNA molecules. The limited success at crystallization explains in part the smaller number of RNA-only structures in the Protein Data Bank. Several approaches have been developed to aid the formation of well-ordered RNA crystals. The majority of these are construct-engineering techniques that aim to introduce crystal contacts to favor the formation of well-diffracting crystals. A typical example is the insertion of tetraloop–tetraloop receptor pairs into non-essential RNA segments to promote intermolecular association. Other methods of promoting crystallization involve chaperones and crystallization-friendly molecules that increase RNA stability and improve crystal packing. In this review, we discuss the various techniques that have been successfully used to facilitate crystal packing of RNA molecules, recent advances in construct engineering, and directions for future research in this vital aspect of RNA crystallography.

Highlights

  • Structural biology of RNA molecules began in the 1960s with the stepwise resolution improvement of the yeast tRNAPhe crystal structures [1,2,3]

  • The tRNA crystal structures unveiled how specific tertiary interactions maintain the three-dimensional fold of the RNA molecule, and how the three-dimensional architecture enables its role in protein translation

  • The GAAC/GAAC Loop and Its 20-nts Receptor (GAAC-R) loop to stem interaction may have a different orientation compared to that formed by GAAA/GAAA Loop and Its 11-nts Receptors (GAAA-R)

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Summary

Introduction

Structural biology of RNA molecules began in the 1960s with the stepwise resolution improvement of the yeast tRNAPhe crystal structures [1,2,3]. The breakthrough came in the crystal structures of the ribozymes [4,5,6] and self-splicing introns [7], which demonstrated how RNA can fold into an architecture capable of carrying out enzymatic catalysis. These early RNA crystal structures set the stage for the structural investigation of large RNA-containing macromolecular complexes such as the ribosome and the spliceosome that are key players in the central dogma of molecular biology [8,9,10]. Crystallization of RNA molecules for structural determination and molecular interaction elucidation is often more challenging than the crystallization of soluble proteins [12,13]. This review may be of interest to nucleic acid crystallographers who seek to expand their repertoire of engineering tools to tackle the crystallization of challenging RNA targets

The Propensity of RNA Helices to Form Intermolecular Stacks
Hairpin Loops and Their Utility in Crystal Packing Design
Promoting Loop-Loop Crystal Contacts
Promoting Loop to Stem Crystal Contacts
Designing Lateral Contacts between Duplexes
Kissing Loop with Two Bulged Purines
Paromomycin Binding Motif
G-Quadruplex
Introducing RNA Binding Proteins
RNA Binding Protein—U1A
Antibody Fragment
Peptide Nucleic Acid
Post-Crystallization Treatment
Future Directions of RNA Crystallography
Future Relevance of Engineering Crystal Packing in RNA Structures
Findings
10. Conclusions
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