In a recent issue of The Journal of Chemical Physics, published by the American Institute of Physics (AIP), a group of scientists at the University of California, Berkeley and Los Alamos National Laboratory describe the first comprehensive, molecular-level numerical study of gene treatment. Their work should help researchers design new experimental gene therapies and possibly solve some of the problems linked to this promising technique.

"There are several barriers to gene delivery," says Nikolaos Voulgarakis of Berkeley, the main author on the paper. "The genetic material must be protected during transit to a cell, it must pass into a cell, it must survive the cell's defense mechanisms, and it must enter into the cell's guarded nucleus".

If all of these barriers can be overcome, gene treatment would be a valuable technique with profound clinical implications. It has the potential to correct many human diseases that result from specific genes in a person's DNA makeup not functioning properly -- or at all. Gene treatment would provide a mechanism to replace these specific genes, swapping out the bad for the good. If doctors could safely do this, they could treat or even cure diseases like cystic fibrosis, certain types of cancer, sickle cell anemia, and many rare inherited disorders.

Safety is a primary concern when working with gene treatment. Some of the first attempts at gene treatment used viruses to insert DNA into cells -- something that viruses naturally do anyway. Viruses can be dangerously toxic, however, and this fact was tragically demonstrated a decade ago when an 18-year-old boy enrolled in a gene treatment study had a massive immune reaction to the viruses used. He died just a few days into the therapy from multiple organ failure, precipitating an immediate halt to the trial.

Since then, a number of alternatives to viruses have emerged for use in gene treatment, including synthetic molecules like "dendrimers," a word that derives from the Greek word for "tree." Similar to trees, dendrimers are branching molecules that are slightly positively charged. This allows them to be loaded with DNA (which is slightly negative charged) for insertion into a cell.

Dendrimers seem to offer a number of advantages over viruses. They appears to be much less toxic, and they may offer other advantages in terms of cost, ease of production, and the ability to transport very long genes. If they can be designed to efficiently -- and safely -- shuttle genes into human cells, then they appears to be a more practical solution to gene treatment than viruses.

So far, laboratory experiments with different types of dendrimers have shown that they can insert genes into cells, but only with very low efficiency. Hoping to discover the key to improving this efficiency, Voulgarakis and colleagues simulated the detailed, atomic-level physical process of dendrimers entering cells. They varied parameters like the dendrimer size and the length of the DNA they carry. Modeling these parameters on a computer is a fast, inexpensive approach for testing different ideas and optimizing the delivery vehicle.

What they uncovered were the key factors that determine the success of dendrimers as gene delivery vehicles -- things like the charges of the dendrimers and their target cell membranes, the length of DNA, and the concentration of surrounding salt. Their work has illuminated some of the molecular-level details that should help clinicians design the most appropriate gene vectors.

"Our study indicates that, over a broad range of biological conditions, the dendrimer/nucleic acid package will be stable enough to remain on the surface of the cell until translocation," says Voulgarakis.

Dendrimers are also used clinically for delivering cancer drugs to tumors, and for helping to image the human body. In the future, Voulgarakis and colleagues plan to study the possibility of using dendrimers as drug delivery vehicles.


Posted by: Emily    Source

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