MadSci Network: Biophysics |
Hello!! What an interesting question, and one often disussed in biophysics. If I had to weigh in on a certain side it would be that of your father, after all, mathematics will explain most (but certainly not all) things in biophysics. Regarding the weights of the bases, this has very little effect on the helical structure of DNA since the bases are similar in mass. How those bases interact, number of torsion angles, their electron clouds, and many other considerations are of importance though. I will address this question with the assumption that you know the structure of standard B-DNA (derived by Watson and Crick) which will be my reference point. Lets look at what type of interactions are taking place: 1) Base Stacking This occurs between the aromatic bases of the nucleic acids with the hydrophobic faces orienting themselves along the helical axis creating a hydrophobic interior to the helix. This is evident by intercalation of hydrophobic molecules such as ethidium bromide into the helix interior. Base stacking plays a predominant role in the melting and annealing of DNA. 2) Hydrogen Bonds Hydrogen bonds play an important role in the structure of DNA. For every C-G base pair there are three H-bonds and for every T-A base pair there are two, assuming Watson-Crick pairing. This is important in holding the two strands together as well since there are usually a significant number of H-bonds along the length of the helix contributing to its stability. 3) Electrostatic Interactions Remember, on each base there is a phosphate oriented towards the outside of the helix. Each base pair has two phosphate groups at a distance of approximately 1.7Angstroms (same side of the chain). The high electronegativity of the phosphates is usually screened by cations in the solution. They are essentially screened from one another by the solvent. Some cations bind tighter (Mg++) then others (K+ for example) lighter to the minor groove of B-DNA though the phosphates almost always remain partially negatively charged. This is evident by single stranded DNA (phosphates farther apart) is favored in low-salt conditions while double stranded DNA(phosphates closer) is favored in high-salt conditions. The latter brings about another factor, solvent interaction. Macromolecular structure is highly dependent on the solution in which it resides. Hydrophobicity, pH, temperature, salinity, etc. all play an important role in helping 'determine' macromolecular structure. As you can see, it is very complex. The fact that DNA forms a double helix is not dependent on base molecular weights or the Fibonacci sequence. Rather, it is a complex culmination of several factors. We simply can't point to one factor that strictly determines tertiary structure of a protein or DNA organization. This is evident by the plethora of analytical and theoretical techniques currently in use to 'predict' structure. Hope this answers your question. If not, just post back to MadSci asking for me. cheers, /frank hays REFERENCES: Principles of Physical Biochemistry, van Holde, Johnson, and Ho: 1998 Prentice Hall ISBN 0-13-720459-0 http://www.ic r.ac.uk/structbi/computing/linux_res.html http://www.se.iucr .org/struc/linux/structure.html
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