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6V6R

Crystal Structure of a Bromine Derivatized Self-Assembling DNA Crystal Scaffold with Rhombohedral Symmetry.

Summary for 6V6R
Entry DOI10.2210/pdb6v6r/pdb
Related6U40 6UAL 6UDN 6UEF
DescriptorDNA (5'-D(*CP*AP*CP*TP*GP*AP*CP*TP*CP*AP*TP*GP*CP*TP*CP*AP*TP*CP*TP*GP*A)-3'), DNA (5'-D(P*AP*GP*CP*AP*TP*GP*A)-3'), DNA (5'-D(*TP*GP*TP*CP*AP*GP*AP*TP*G)-3'), ... (5 entities in total)
Functional Keywordsself-assembly, dna nanotechnology, dna scaffold, crystal lattice, dna, bromine, sad, bromo-du
Biological sourcesynthetic construct
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Total number of polymer chains4
Total formula weight13069.42
Authors
Simmons, C.R.,MacCulloch, T.,Stephanopoulos, N.,Yan, H. (deposition date: 2019-12-05, release date: 2020-12-09, Last modification date: 2024-03-06)
Primary citationSimmons, C.R.,MacCulloch, T.,Zhang, F.,Liu, Y.,Stephanopoulos, N.,Yan, H.
A Self-Assembled Rhombohedral DNA Crystal Scaffold with Tunable Cavity Sizes and High-Resolution Structural Detail.
Angew.Chem.Int.Ed.Engl., 59:18619-18626, 2020
Cited by
PubMed Abstract: DNA is an ideal molecule for the construction of 3D crystals with tunable properties owing to its high programmability based on canonical Watson-Crick base pairing, with crystal assembly in all three dimensions facilitated by immobile Holliday junctions and sticky end cohesion. Despite the promise of these systems, only a handful of unique crystal scaffolds have been reported. Herein, we describe a new crystal system with a repeating sequence that mediates the assembly of a 3D scaffold via a series of Holliday junctions linked together with complementary sticky ends. By using an optimized junction sequence, we could determine a high-resolution (2.7 Å) structure containing R3 crystal symmetry, with a slight subsequent improvement (2.6 Å) using a modified sticky-end sequence. The immobile Holliday junction sequence allowed us to produce crystals that provided unprecedented atomic detail. In addition, we expanded the crystal cavities by 50 % by adding an additional helical turn between junctions, and we solved the structure to 4.5 Å resolution by molecular replacement.
PubMed: 32533629
DOI: 10.1002/anie.202005505
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.7 Å)
Structure validation

237735

数据于2025-06-18公开中

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