Molecular structure of nicked DNA: A substrate for DNA repair enzymes
- 1. Massachusetts Institute of Technology, Cambridge (USA)
- 2. Leiden State Univ. (Netherlands)
- 3. Univ. of Illinois, Urbana-Champaign (USA)
Description
The molecular structure of a nicked dodecamer DNA double helix, made of a ternary system containing d(CGCGAAAACGCG) + d(CGCGTT) + d(TTCGCG) oligonucleotides, has been determined by x-ray diffraction analysis at 3 angstrom resolution. The molecule adopts a B-DNA conformation, not unlike those found in intact dodecamer DNA molecules crystallized in a somewhat different crystal lattice, despite a gap due to the absence of a phosphate group in the molecule. The helix has a distinct narrow minor groove near the center of the molecule at the AAAA region. This suggests that the internal stabilizing forces due to base stacking and hydrogen-bonding interactions are sufficient to overcome the loss of connectivity associated with the disruption of the covalent backbone of DNA
Additional details
Publishing Information
- Journal Title
- Proceedings of the National Academy of Sciences of the United States of America
- Journal Volume
- 87
- Journal Issue
- 7
- Series
- Proc. Natl. Acad. Sci. U.S.A.
- Journal Page Range
- 2526-2530
- ISSN
- 0027-8424
- CODEN
- PNASA
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 22034250
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CHEMICAL BONDS; DNA; DNA REPAIR; FOURIER ANALYSIS; LIQUID COLUMN CHROMATOGRAPHY; MOLECULAR STRUCTURE; NUCLEOTIDES; STEREOCHEMISTRY; STRAND BREAKS; X-RAY DIFFRACTION
- Descriptors DEC
- BIOLOGICAL RECOVERY; BIOLOGICAL REPAIR; CHROMATOGRAPHY; COHERENT SCATTERING; DIFFRACTION; NUCLEIC ACIDS; ORGANIC COMPOUNDS; SCATTERING; SEPARATION PROCESSES