The Structure of Double-Stranded Dna

Structure of a DNA quadruplex

As mentioned above, the two individual strands are held together by hydrogen bonds between individual T·A and C·G base pairs. In DNA, the distance between the atoms involved is 2.8 to 2.95 angstroms (10−10 meters). While individually weak, the large number of hydrogen bonds along a DNA chain provides sufficient stability to hold the two strands together.

The stabilization of duplex (double-stranded) DNA is also dependent on base stacking. The planar, rigid bases stack on top of one another, much like a stack of coins. Since the two purine.pyrimidine pairs (A.T and C.G) have the same width, the bases stack in a rather uniform fashion. Stacking near the center of the helix affords protection from chemical and environmental attack. Both hydrophobic interactions and van der Waal's forces hold bases together in stacking interactions. About half the stability of the DNA helix comes from hydrogen bonding, while base stacking provides much of the rest.Double-stranded DNA in its canonical B-form is a right-handed helix formed by two individual DNA strands aligned in an antiparallel fashion (a right-handed helix, when viewed on end, twists clockwise going away from the viewer). Antiparallel DNA has the two strands organized in the opposite polarity, with one strand oriented in the 5′-3′ direction and the other oriented in the 3′-5′ direction.

In the right-handed B-DNA double helix, the stacked base pairs are separated by about 3.24 angstroms with 10.5 base pairs forming one helical turn (360°), which is 35.7 angstroms in length. Two successive base pairs, therefore, are rotated about 34.3° with respect to each other. The width of the helix is 20 angstroms. An idealized model of the double helix is shown in Figure 3. As can be seen, the organization of the bases creates a major groove and a minor groove.

Adenine and thymine are said to be complementary as are cytosine and guanine. Complementary means "matching opposite." The shapes and charges of adeninne and thymine complement each other, so that they attract one another and link up (as do cytosine and guanine). Indeed, one entire strand of duplex DNA is complementary to the opposing strand. During replication, the two strands unwindand each serves as a template for formation of new complementary strand, so that replication ends with two exact double-stranded copies.

Why is DNA called the Blueprint of Life?

Every cell in your body has the same "blueprint" or the same DNA. Like the blueprints of a house tell the builders how to construct a house, the DNA "blueprint" tells the cell how to build the organism. Yet, how can a heart be so different from a brain if all the cells contain the same instructions? Although much work remains in genetics, it has become apparent that a cell has the ability to turn off most genes and only work with the genes necessary to do a job. We also know that a lot of DNA apparently is nonsense and codes for nothing. These regions of DNA that do not code for proteins are called "introns", or sometimes "junk DNA". The sections of DNA that do actually code from proteins are called "exons".

Functional neuroimaging

Functional neuroimaging is the use of neuroimaging technology to measure an aspect of brain function, often with a view to understanding the relationship between activity in certain brain areas and specific mental functions.

It is primarily used as a research tool in cognitive neuroscience and neuropsychology.

Common methods include positron emission tomography (PET), functional magnetic resonance imaging (fMRI), multichannel electroencephalography (EEG) or magnetoencephalography (MEG), and near infrared spectroscopic imaging (NIRSI).

PET, fMRI and NIRSI can measure localized changes in cerebral blood flow related to neural activity..
(http://www.sciencedaily.com/articles/f/functional_neuroimaging.htm)

Functional neuroimaging

Functional neuroimaging is the use of neuroimaging technology to measure an aspect of brain function, often with a view to understanding the relationship between activity in certain brain areas and specific mental functions.

It is primarily used as a research tool in cognitive neuroscience and neuropsychology.

Common methods include positron emission tomography (PET), functional magnetic resonance imaging (fMRI), multichannel electroencephalography (EEG) or magnetoencephalography (MEG), and near infrared spectroscopic imaging (NIRSI).

PET, fMRI and NIRSI can measure localized changes in cerebral blood flow related to neural activity..
(http://www.sciencedaily.com/articles/f/functional_neuroimaging.htm)