Abstract
In order to investigate the relationship existing between the electronic structures of collagen and its biochemical functions in vivo, the semiempirical CNDO/2 SCF MO calculations were carried out on several model polymers of collagen, (Gly-Pro) n, (Gly-Hyp) n, (Ala-Pro) n, (Ala-Hyp) n, (Gly-Pro-Gly) n, (Gly-Hyp-Gly) n, (Gly-Pro-Pro) n and (Gly-Pro-Hyp) n. Geometries of the skeleton of these polymers were assumed to be the same as those of poly( l-proline) I ( cis) and II ( trans) and the calculations were performed only on infinite polymers in a single chain. The results show that the cis form is always more stable than the trans form for all the polymers treated. This energy difference between the cis and trans forms depends, for example, on the kind of amino acid residue, Gly or Ala, but this could not be seen in the Pro or Hyp residue. The flexibility or mobility of the collagen structure was explained using the energy difference between the cis and trans forms of the polymers, i.e. the cis-trans conversion of the collagen was discussed in connection with the energy difference. The reason why the collagen has the constitution of (Gly-Pro-Hyp) n is briefly discussed.
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