The Double Helix

Submitted by ChemPRIME Staff on Thu, 01/13/2011 - 14:01

There is more to the structure of DNAAbbreviation for deoxyribonucleic acid; the polymer of nucleotides that constitutes the genetic material of chromosomes. than just the primary sequence of nitrogenous bases. Secondary structureThe folding of a protein into sheets and helices held in their shape primarily by hydrogen bonding. also plays a crucial biochemical role. Each DNA moleculeA set of atoms joined by covalent bonds and having no net charge. consists of two nucleotideAn organic compound consisting of a purine or pyrimidine base bonded to a sugar that is bonded to a phosphate group; a monomer for DNA or RNA. chains wrapped around each other in a double helix and held together by hydrogen bonds. This hydrogen bonding involves only the nitrogenous bases. Each of the purine bases can hydrogen bond with one and only one of the pyrimidine bases.

Thus adenine can hydrogen bond with thymine and guanine with cytosine, as shown in Fig. 1. Note that in both cases there is an exact match of hydrogen atomsThe smallest particle of an element that can be involved in chemical combination with another element; an atom consists of protons and neutrons in a tiny, very dense nucleus, surrounded by electrons, which occupy most of its volume. on the one base with nitrogen or oxygen atoms on the other. Note also that the distance from sugarA small carbohydrate that either contains five or six carbon atoms or is a dimer of two units, each containing five or six carbon atoms. linkage to sugar linkage across each of the base pairs in Fig. 1 is almost exactly the same. This explains why only these two combinations occur in DNA. Other combinations (i.e., adenine-cytosine) are not nearly so favorable energetically.
Figure 1 Hydrogen-bonded base pairs of DNA. Note the nearly equal separations between paints where the bases connect to sugars in the DNA backbone. A pair of purines would have much larger and a pair of pyrimidines much smaller separation, making it difficult for such pairs to fit between the two strands.


The overall geometry of the two nucleotide chains in the DNA molecule is in the form of the double helix shown in Fig. 2. Each helix corresponds to a nucleotide chain, and the two chains are joined throughout their length by adenine-thymine or guanine-cytosine pairs. These base pairs are stacked one above the other with their planes perpendicular to the axis of the two spirals. This places the hydrophobicWater-hating; not attracted to water molecules or polar molecules. base pairs inside the structure and allows the hydrophilicWater-loving; attracted to water molecules and polar molecules. sugar and phosphate groups to contact water on the exterior. The whole helix will just fit inside a cylinder 2000 pm in diameter.

Figure 2 The double helix of DNA. Three different representations are shown. At the bottom the atoms are shown as space-filling spheres; in the middle the sugar and phosphate groups are identified by S and P and the nitrogenous bases by A, C, G, and T. In the topmost section the base pairs are represented by crossbars.

The spacing between base pairs is 340 pm, and there are 10.5 base pairs in one full turn of the helix.

The two nucleotide chains in the double helix are said to be complementary to each other. Because of the exact pairing of the bases we can always tell the sequences of bases in the one chain from that in the other. Thus if the first six bases in one chain are AGATCC, we know that the first six bases in the other will be TCTAGG. Both chains are therefore alternative representations of the same information. If one or two bases become misplaced in either strand, this can be recognized because of mismatching with the complementary strand. Repair enzymes can then correct the sequence of bases along the incorrect strand. A final point to make is that the two strands are antiparallel. This means that one strand, from bottom to top is going from the 5'carbon to the 3' carbon, while the complimentary strand is going 3' to 5' from bottom to top.

This double-helix model for DNA was first suggested in 1953 by James D. Watson (born 1928) and Francis Crick (1916 to 2004). It was an important milestone in the history of science, since it marked the birth of a new field, molecular biology, in which the characteristics of living organisms could at last begin to be explained in terms of the structure of their molecules. In 1962 Crick and Watson shared the Nobel Prize with M. F. H. Wilkins, whose x-rayA high-energy form of electromagnetic radiation that has sufficient energy to ionize inner electrons from an atom. crystallographic data had helped them to formulate their model. Rosalind Franklin(1920-1958) who performed the x-ray crystallography experiments did not win the Nobel Prize, as they are not awarded posthumously, but should be included in any discussion on the discovery of the double helix. A fascinating account of this discovery, which does not always put the author in a favorable light, can be found in Watson’s book “The Double Helix.“