Nucleic Acid Crystallography Volume II

A special issue of Crystals (ISSN 2073-4352). This special issue belongs to the section "Biomolecular Crystals".

Deadline for manuscript submissions: 31 December 2024 | Viewed by 3448

Special Issue Editor


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Guest Editor
Department of Biochemistry and Physiology, College of Medicine, University of Oklahoma Health Sciences, Oklahoma City, OK 73104-5419, USA
Interests: RNA editing; RNA structure; SAD phasing methods; direct methods phasing; crystal size optimization; molecular modeling
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Special Issue Information

Dear Colleagues,

The deposition of the structures of nucleic acid and nucleic acid–protein complexes in the Protein Databank continues to grow due to improvements in the methods for synthesis, purification, crystallization, and structure determination. However, the ratio between the number of nucleic acid-containing structures and that of protein structures is 1:14. This ratio does not reflect the importance of nucleic acids, especially with the recent identification of new roles played in biology by noncoding RNAs. This Special Issue provides a platform for updates on the developments and trends in nucleic acid crystallography. The scope includes X-ray, neutron, and electron diffraction (microED) methods as well as small-angle scattering methods. We seek original research reports and review articles focused on specific aspects of nucleic acid crystallography, including but not limited to the following topics:

  • New crystal structures containing nucleic acids, including complexes with drugs, proteins, or metals;
  • Small angle scattering studies;
  • Crystallization construct design;
  • Large-scale chemical or enzymatic synthesis of nucleic acids;
  • Nucleic acid purification for crystallographic studies;
  • Crystallization screen design;
  • Use of biophysical methods to screen crystallization constructs;
  • Crystal size optimization;
  • Optimization of diffraction quality;
  • Crystal derivatization with heavy atoms;
  • Heavy-atom incorporation in synthetic RNA and DNA;
  • Engineering of nucleic acids to promote crystallization;
  • The use of crystallization chaperones, including RNA nanobodies;
  • The use of fusions to ease purification or promote crystallization;
  • The use of ligands to promote crystallization;
  • Post-crystallization crystal improvement (crystal hardening);
  • Cryocrystallography;
  • Room-temperature data collection with synchrotron radiation;
  • New diffraction methods (e.g., serial crystallography, XFELS, radiation damage);
  • Crystal twinning;
  • Crystal packing disorder;
  • Pseudosymmetry;
  • Diffuse scattering;
  • Phasing methods;
  • Density map interpretation;
  • Model building in electron density maps;
  • Structure refinement method advancements;
  • Error analysis of nucleic acid structures;
  • Methods of comparing crystal structures;
  • Molecular dynamics simulations in crystal lattices;
  • Use of machine learning to facilitate crystallization;
  • Integrative molecular modeling that includes crystal structures of nucleic acids;
  • Use of modeling methods to improve the diffraction quality;
  • Molecular visualization of RNA, DNA or both;
  • Structural bioinformatics using crystal structures of nucleic acids;
  • Use of crystallography in DNA and RNA nanotechnology;
  • Nucleic acid–water interactions in crystal structures.

Prof. Dr. Blaine Mooers
Guest Editor

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Keywords

  • nucleic acid synthesis and purification
  • RNA and DNA crystallization
  • RNA and DNA crystal improvement
  • Nucleic acid diffraction studies
  • RNA and DNA structure determination
  • RNA and DNA model building
  • nucleic acid structure analysis
  • nucleic acid structural bioinformatics

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Published Papers (2 papers)

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17 pages, 2946 KiB  
Article
Extending Ab Initio Phasing up to 2.2 Å Resolution: New Superposition Techniques
by Maria Cristina Burla, Benedetta Carrozzini, Giovanni Luca Cascarano, Carmelo Giacovazzo and Giampiero Polidori
Crystals 2023, 13(6), 874; https://doi.org/10.3390/cryst13060874 - 26 May 2023
Cited by 1 | Viewed by 753
Abstract
Patterson superposition techniques are a historical method for solving the structures of small molecules ab initio, provided they contain heavy atoms in the unit cell. In the 1990s, they were combined with effective EDM procedures and succeeded in the crystal structure solution of [...] Read more.
Patterson superposition techniques are a historical method for solving the structures of small molecules ab initio, provided they contain heavy atoms in the unit cell. In the 1990s, they were combined with effective EDM procedures and succeeded in the crystal structure solution of macromolecular structures with resolution data up to 1.6–1.9 Å. In this paper we enlarge the concept of Patterson superposition by replacing it with the vector superposition concept. We show, indeed, that besides Patterson other Fourier syntheses may also be used for the superposition of the interatomic vectors. Five Fourier syntheses are described and used in the practical applications. We show that even macromolecular structures with 2.2 Å data resolution may be solved via the new approach. Full article
(This article belongs to the Special Issue Nucleic Acid Crystallography Volume II)
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16 pages, 4158 KiB  
Article
Structural Characterization of Alzheimer DNA Promoter Sequences from the Amyloid Precursor Gene in the Presence of Thioflavin T and Analogs
by Hristina Sbirkova-Dimitrova, Rusi Rusew, Nikola Kuvandjiev, Annie Heroux, Tzanko Doukov and Boris L. Shivachev
Crystals 2022, 12(12), 1717; https://doi.org/10.3390/cryst12121717 - 26 Nov 2022
Viewed by 1959
Abstract
Understanding DNA–ligand binding interactions requires ligand screening, crystallization, and structure determination. In order to obtain insights into the amyloid peptide precursor (APP) gene–Thioflavin T (ThT) interaction, single crystals of two DNA sequences 5′-GCCCACCACGGC-3′ (PDB 8ASK) and d(CCGGGGTACCCCGG)2 (PDB 8ASH) were grown in [...] Read more.
Understanding DNA–ligand binding interactions requires ligand screening, crystallization, and structure determination. In order to obtain insights into the amyloid peptide precursor (APP) gene–Thioflavin T (ThT) interaction, single crystals of two DNA sequences 5′-GCCCACCACGGC-3′ (PDB 8ASK) and d(CCGGGGTACCCCGG)2 (PDB 8ASH) were grown in the presence of ThT or its analogue 2-((4-(dimethylamino)benzylidene)amino)-3,6-dimethylbenzo[d]thiazol-3-ium iodide (XRB). Both structures were solved by molecular replacement. In the case of 8ASK, the space group was H3 with unit cell dimensions of a = b = 64.49 Å, c = 46.19 Å. Phases were obtained using a model generated by X3DNA. The novel 12-base-pair B-DNA structure did not have extra density for the ThT ligand. The 14-base-pair A-DNA structure with bound ThT analog XRB was isomorphous with previously the obtained apo-DNA structure 5WV7 (space group was P41212 with unit cell dimensions a = b = 41.76 Å, c = 88.96 Å). Binding of XRB to DNA slightly changes the DNA’s buckle parameters at the CpG regions. Comparison of the two conformations of the XRB molecule: alone and bound to DNA indicates that the binding results from the freedom of rotation of the two aromatic rings. Full article
(This article belongs to the Special Issue Nucleic Acid Crystallography Volume II)
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