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Designing drugs
If we take diabetes disease as an example, for years diabetes patients were treated with insulin
derived from the pancreas glands of animals such as pigs and cows. Although insulin derived
from these animals is similar to human generated insulin, their composition was slightly
different, causing a number of patients immune systems to produce antibodies against it. This
led researchers to focus on model organisms to synthesize human insulin based on the insulin
gene identified at that time.
Model organisms & Recombinant DNA technology
Model organisms are non-human species, which are extensively studied to understand biological
phenomenon and are used as in vivo models to experiment on human diseases. These model
organisms are identified as a possible solution to produce drugs such as insulin protein to treat
the aforementioned forms of diseases.
The central dogma of molecular biology suggests that, in order to produce a protein, the DNA
that codes for the protein should be translated and transcribed. If a drug (a required protein) is to
be produced with a model organism, the DNA coding for the required protein should be included
in the genome of that organism. In order to achieve that, the cell of that model organism will be
genetically engineered by inserting the DNA coding sequence of the corresponding gene to a
model organisms DNA molecule. The technology carrying out this process is called the
Recombinant DNA technology.
After combining the DNA sequences, the central dogma of molecular biology takes care of
synthesizing the required protein. That is, the combined DNA sequence will be transcribed to
mRNA, which will be translated to produce the proteins. The required protein should then be
isolated and purified to acquire the final outcome, which will be the medication to treat the
diseases such as diabetes.
Bibliography
http://members.tripod.com/diabetics_world/lillys_rdna_insulin.htm
http://www.youtube.com/watch?v=8rXizmLjegI&list=LLw_LwaVhkpDcWNO3LJpsJHg
Group Members
2009/CS/180 M. J. M. Shazan
2009/CS/128 W. L. Ranaweera
2009/S/11340 N. S. Rubasinghe