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Study explores limits of DNA structure and function, may expand use of modified DNA in medicine

Scientists from IOCB Prague are pushing the limits of DNA
Credit: Nucleic Acids Research (2023). DOI: 10.1093/nar/gkad893

A team led by Professor Michal Hocek at IOCB Prague has explored the limits of the structure and function of DNA and successfully pushed forward known boundaries. Their latest research has just been published in Nucleic Acids Research.

They prove that even heavily modified double helices of DNA are stable enough to be used for special applications. This discovery might expand the possibilities of utilizing modified DNA, for example, in medicine.

DNA consists of two long negatively charged chains that hold together even though they repel each other. This is made possible by what is known as stacking interactions and base pairing. Hocek and his colleagues advanced the known limits when they modified DNA by adding an extra negative charge to each letter of the genetic code.

This doubled the , yet the DNA remained stable. They also found that such modified DNA not only holds together but that it can also be synthesized or replicated and sequenced using the enzyme DNA polymerase.

"Think of DNA as a scaffold on which you can attach various chemical compounds with different functions. These are , such as side chains of amino acids, which occur naturally only in peptides and proteins," says Hocek.

"In current medicine, we are able to use these only to a relatively limited extent. The reason is that they are markedly unstable and get decomposed rapidly when inside an organism. One solution to this would be a stable skeleton to which they could be firmly attached. And DNA could be just such a base structure in the future.

"The aim of this research is to create DNA molecules that will mimic other chemical compounds. This would enable us to leverage the medicinal potential of certain biomolecules that are difficult to retain in the body. Examples of such biomolecules are the already mentioned peptides or proteins."

The Hocek group has already made significant progress, although research in this direction is at its beginning worldwide. The team has, for example, succeeded in developing a novel modified aptamer, which is a short DNA sequence that can bind to a specific target molecule, most frequently a protein.

Aptamers have similar properties to antibodies, but they are much more stable. For this reason, aptamers can potentially replace antibodies employed in medicine. However, the number of approved therapeutic aptamers globally can still be counted on the fingers of one hand.

The current research exploring the limits of DNA is part of a larger project led by Hocek. This is the second time its results have drawn interest from the journal Nucleic Acids Research. Previously, scientists from IOCB Prague published a method for the enzymatic synthesis of fully artificial DNA. During this synthesis, all nucleotides forming natural DNA are replaced by their modified versions with attached hydrophobic (i.e., water-repelling) molecules.

More information: Natalia Kuprikova et al, Superanionic DNA: enzymatic synthesis of hypermodified DNA bearing four different anionic substituents at all four nucleobases, Nucleic Acids Research (2023). DOI: 10.1093/nar/gkad893

Journal information: Nucleic Acids Research

Citation: Study explores limits of DNA structure and function, may expand use of modified DNA in medicine (2023, November 9) retrieved 16 April 2024 from
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