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THE MOLECULE

In the autumn of 1951, James Watson (left) and Francis Crick (right) started work on
unravelling the structure of DNA. It was known at the time that DNA was present in the
nucleus of every living cell, and that it had something to do with heridity, but without
a knowledge of its structure little more could be understood about how it actually
worked. They approached the problem with the same methodology that had been pioneered by
Linus Pauling, who after years of exhaustive study had earlier discovered that many
proteins exhibited a helical structure. Their task was to devise a structure which would
account for all the chemical and X-ray evidence, and at the same time be consistent with
all the structural features of the units involved - such as the size and shape, bond
angles and lengths, configurations and conformations. X-ray diffraction photographs of
DNA fibres taken by Rosalind Franklin and Maurice Wilkins showed a distinctive X-shape,
which was characteristic of a helix structure, but strong arcs on the meridian indicated
a repeating structure 3.4 A apart. And from the chemical evidence, it was known that part
of the structure was comprised of 4 heterocyclic bases, adenine (A), guanine (G),
cytosine (C) and thymine (T), somehow linked together with sugar units and phosphates.
One of the biggest puzzles was that although the proportion of these bases varied from
one DNA to another, it was always found that the number of A = T, and G = C.
Adenine 
Guanine 
Cytosine 
Thymine 
The 4 bases which make up DNA
(Click on each image to get its 3D molfile). 
Using molecular models, Watson and Crick devised a structure in which all of the building
blocks fitted together without crowding or overlapping, and which permitted a great deal
of stabilisation by Hydrogen bonds. Moreover, these Hydrogen bonds were of the kind that
Pauling had shown to be the strongest and therefore the most important for determining
structure in proteins, namely N-H-N or N-H-O.
In April 1953 Watson and Crick published their structure - the now famous double helix.
This brilliant accomplishment ranks as one of the most significant discoveries in science
because it led the way to an understanding of genetics in terms of the molecules
involved. In 1962 they received the Nobel prize for Medicine in recognition of this
achievement, along with Maurice Wilkins of Kings College London who had performed the
initial X-ray crystallography studies.
A very small section of DNA showing the double helix structure linked by bases, like the
rungs on a twisted ladder.
(Click here or on the image to get 3D structure in Molfile format).
(Click here to get an interactive 3D structure in pdb format - requires Chime). 
Bases, Nucleotides and Nucleosides
In every living cell there are found nucleoproteins - substances made up of proteins
combined with natural polymers, the nucleic acids. Where the backbone of a protein
molecule is a polyamide (or polypeptide) chain, the backbone of a nucleic acid molecule
is a polyester chain (called a polynucleotide chain). The ester is derived from
phosphoric acid (the acid portion) and a sugar (the alcohol portion).
Polynucleotide chain
The sugar is D-ribose, which is in the group of nucleic acids called ribonucleic acids
(RNA), and D-2-deoxyribose forms the basis of DNA. The 2-deoxy simply indicates the lack
of an -OH group at the 2 position. Thus DNA stands for deoxyribonucleic acid.
Attached to the carbon at one side of the sugar is one of the 4 bases, A, C, G, or T. The
base-sugar unit is called a nucleoside. Attached to the other side of the sugar is a
phosphoric acid unit, linking the nucleoside to the neighbouring sugar. The
base-sugar-phosphoric acid unit is called a nucleotide.
Adenosine, a nucleotide containing adenine (red), deoxyribose (black) and phosphoric acid
(blue).
The 3D molfiles of all of the 4 nucleotides can be obtained here: A, C, G, T.
Two of these polynucleotide chains, which can be many millions of nucleotides long, then
wrap around one another to form the double helix structure, with every A group H-bonding
to the T group on the adjacent chain (see here for A-T molfile), and every G group
H-bonding to its matching C group (see here for G-C molfile).
DNA - the source of heredity
The double helix of DNA controls heredity on the molecular level. The hereditary
information is stored as the sequence of bases along the polynucleotide chain - a message
written in a language of only 4 letters, A, C, G and T. DNA both preserves this
information, and uses it. It does this through 2 properties:
DNA molecules can duplicate themselves, in a process called replication, in which the 2
halves of the helix separate and a new partner is fabricated to exactly match each half.
DNA molecules control the synthesis of the proteins which characterise each type of
organism. The structure of DNA directly controls the structure of proteins, and the
structure of proteins directly determines the way in which they control living processes.
It would appear that biology is increasingly becoming a matter of the shapes and sizes of
molecules.
DNA Fingerprinting
Since the DNA within any species, and to any individual within that species, is unique,
it can be used as a means of identification. DNA can be extracted from organic remains
(blood, saliva, etc) left at crime scenes to identify the criminal. It can also be used
to determine parentage, the gender of animals and birds (where it is difficult to do so
by just looking at them!), and to prove whether traditional medicines contain extracts
from endangered species. This process is called DNA fingerprinting.
Bibliography
The Path to the Double Helix: The Discovery of DNA, Robert C. Olby (Dover Pubns; ISBN:
0486681173, 1994) 
Organic Chemistry, Morrison and Boyd (Allyn and Bacon, Boston, 1983). 
Biochemistry, L. Stryer (Freeman, San Francisco, 1975). 
Interactive DNA structure (Imperial College, requires Chime) 
Interactive DNA Structure from the University of Massachusetts (requires Chime). 
The Curtis model of H-bonding in the T-A and C-G base pairs (Imperial College London,
requires Chime). 

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