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  Home > JCE Print > Journal of Chemical Education > Issues > 2007  > August  >
In the Laboratory
JCE Featured Molecules
Molecular Models of DAPI
William F. Coleman
Department of Chemistry, Wellesley College, Wellesley, MA 02481
Cover
August 2007
Vol. 84 No. 8
p. 1307

Full Text
This month’s Featured Molecule is DAPI (4′,6-diamidino-2-phenylindole), from the paper by Eamonn F. Healy (1). The utility of DAPI is a consequence of its being a minor-groove binder to DNA. A crystal structure of DAPI binding to the minor groove of a synthetic DNA has been determined, and the structure file made available through the RCSB Protein Data Bank (2, 3). That structure is also included in the Featured Molecules Collection, with the water molecules removed for the sake of clarity.

DAPI binding to the minor groove of a synthetic DNA.

For many students this may be their first encounter with the binding of small molecules to DNA. Another example of such binding is the intercalation of the antibiotic actinomycin into DNA. The Department of Biology at the University of Hamburg maintains an excellent Web site showing both crystal and NMR structures of actinomycin intercalation (4).

Observant students will also note in the structure of DAPI a theme that has appeared several times in our Featured Molecules, and that is the non-planarity of adjacent delocalized ring systems. In DAPI, it is a five-membered ring adjacent to a six-membered ring, and the observed departure from planarity is less than that in biphenyl. Students might be asked to explain that difference.

Students can examine these structures in Jmol or Chime, along with other molecules in the collection, in the JCE Digital Library.

Literature Cited

  1. Healy, Eamonn F. J. Chem. Educ. 2007, 84, 1304–1307.
  2. RCSB PDB: Structure Explorer (accessed Jun 2007).
  3. Vlieghe, D.; Sponer, J.; Van Meervelt, L. Biochemistry 1999, 38, 16443–16451.
  4. Antibiotics: Actinomycin D—Structure Model (accessed Jun 2007).
More Information
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Citation
Coleman, William F. J. Chem. Educ. 2007, 84, 1307.
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Keywords
Computer-Based Learning; Hands-On Learning / Manipulatives; Nucleic Acids / DNA / RNA; Proteins / Peptides; Upper-Division Undergraduate
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History
Created:
Last Updated:
6/22/2007
7/5/2007
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Experiments, laboratory exercises, lecture demonstrations, and other descriptions of the use of chemicals, apparatus, instruments, computers, and computer interfaces are presented in the Journal of Chemical Education as illustrative of new or improved ideas or concepts in chemistry instruction and are directed at qualified teachers. Although every effort is made to assure and encourage safe practices and safe use of chemicals, the Journal of Chemical Education cannot assume responsibility for uses made of its published materials. Many chemicals are hazardous. Precautions for the safe use of hazardous chemicals and directions for their proper disposal are described in the Material Safety Data Sheets and on the labels. We strongly urge all those planning to use materials from our pages to make choices and to develop procedures for laboratory and classroom safety in accordance with local needs and situations.
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