Sunday Times (Sri Lanka)

One drop of blood test

New technique 'could one day diagnose a myriad of conditions from cancer to diabetes

- By Lizzie Parry

Anew blood test could one day analyze one drop of blood to detect a host of diseases, from cancer to autoimmune conditions.

Scientists at the University of Pittsburgh have developed a unique method for detecting antibodies in the blood of patients.

Their discovery marks a proof-of-principle concept, that could open the door to the developmen­t of simple diagnostic tests for diseases for which no microbial cause is known.

The findings mark the first evidence that it is possible to develop blood tests for any infectious disease by screening random libraries of non-biological molecular shapes.

Dr Donald Burke, dean of the Pitt Graduate School of Public Health, said: 'This "needle-in-a-molecular haystack" approach is a new way to develop diagnostic assays.

'The method does not rely on starting with known viral components.

'This is important because there are conditions for which there isn't a known antigen, such as newly emerged epidemics, autoimmune diseases or even responses to traumatic injury.'

When a person's immune system is faced with an antigen or foreign invader, such as an infectious disease, or even an injury with tissue damage, it responds by producing antibodies.

Like the pieces of a puzzle, specific parts of the surface of these antibodies fit to the shape of the molecules on the invader or the damaged tissue.

The researcher­s used a technique, pioneered by co-author Dr Thomas Kodadek, of the Scripps Research Institute.

It synthesize­s random molecular shapes called 'peptoids' hooked on to microscopi­c plastic beads.

The technique can produce millions of molecular shapes.

The peptoids are not organic, but if they match to the correspond­ing shape on an antibody, that antibody will connect to them, allowing the scientist to pull out that bead and examine that peptoid and its correspond­ing antibody.

Using the technique, Dr Burke and his team chemically generated a huge library of random molecular shapes.

Then, using blood from HIVinfecte­d patients and from non-infected people, the researcher­s screened a million of these random molecular shapes to find the ones that bound only to antibodies present in the blood of HIV-infected patients, but not the healthy controls.

Then, using blood from HIVinfecte­d patients and from non-infected people, the researcher­s screened a million of these random molecular shapes to find the ones that bound only to antibodies present in the blood of HIV-infected patients, but not the healthy controls.

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