Drug design is the term which refers to
the ingenious process of finding new drug to help the field of medicine. This
drug is usually an organic molecule, which attaches itself to a biomolecule. It
can either obstruct or initiate the biomolecule, resulting in therapeutic
benefit to the patient.
The drug design of the 21st
century is using the computer as helping in making the drug. The essential goal
of Computer Aided Drug Design is to predict whether a particular molecule will
bind itself to the host (and start the process) and if yes, then how strong
will be the bond.
In the field of drug design, molecular
dynamics (MD) is used to study various macromolecules as well as macro-molecule
small molecule interactions. This technique provides dynamic information of
macromolecular processes. Quantitative Structure Activity Relationships (QSAR)
establishes a mathematical correlation between the chemical structures of a set
of compounds as well as biological activities.
Bentham Science Journal “Current Computer-Aided Drug Design” aims to publish all
the latest developments in drug design based on computational techniques. The
field of computer-aided drug design has had extensive impact in the area of
drug design. Current Computer-Aided
Drug Design is an essential journal for all medicinal chemists who
wish to be kept informed and up-to-date with all the latest and important
developments in computer-aided methodologies and their applications in drug
discovery. This journal has an impact factor of 1.54 and is indexed in agencies
like MEDLINE, Pub Med, EMBASE and SCOPUS.
10)
A Possible Cure for Sickle Cell Disease
Sickle Cell Disease (SCD) or Sickle Cell
Anemia (SCA) is a hereditary blood disorder, in which the red blood cells
transform into a ‘sickle’ shape. It disrupts the natural circulation of blood.
This mutation of the red blood cells can be extremely dangerous for the
patients. Not only it can make the patient anemic, it can also reduce the life
expectancy. SCD is hereditary. In simpler words, the cell change their shape
from ‘disc like’ to ‘sickle’ shape when the DNA of a new born baby send signal
to transform the hemoglobin (the Oxygen carrying component of the red blood
cells) from ‘fetal’ to ‘adult’.
Recent studies in the discipline of
Hematology (the study of blood), have proved that the chances of an individual getting SCD can be reduced. According to the research, the
researchers used a specialized tool, a genetically engineered zinc finger (ZF)
protein, which they custom-designed to latch onto a specific DNA site carrying
the code for fetal hemoglobin. They attached the ZF to another protein that
forced a chromatin loop to form. The loop then activated gene expression that
produced embryonic hemoglobin in blood-forming cells from adult mice.
The researchers had the same result when
they experimented on human blood. Now the team of researchers will continue
investigations aimed at moving their research toward clinical application.
Bentham Science Publishers
is one of the leading STM publishers in the industry. It has more than 116
online and print journals, 150 plus Open Access journals, and related
print/online book series. One of the numerous eBooks is, Immunology
of Pregnancy 2013, which is a
complete compendium of gynecological immunology, spanning from fecundation to
delivery.
[This article is based on the news: ‘Flipping a Gene
Switch Reactivates Fetal Hemoglobin, May Reverse Sickle Cell Disease’ by
ScienceDaily.com]
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