© Travis Gallagher, NISTComputer model of the defined structure for the cyclic AMP receptor protein (CRP) found in Mycobacterium tuberculosis.
The bacterium behind one of mankind's deadliest scourges, tuberculosis, is helping researchers at the Commerce Department's National Institute of Standards and Technology (NIST) and the Department of Energy's Brookhaven National Laboratory (BNL) move closer to answering the decades-old question of what controls the switching on and off of genes that carry out all of life's functions.
The NIST/BNL team reports that it has defined - for the first time - the structure of a "metabolic switch" found inside most types of bacteria - the cyclic AMP (cAMP) receptor protein, or CRP - in its "off" state. CRP is the "binding site" (attachment point) for cAMP, a small molecule that, once attached, serves as the signal to throw the switch. This "on" state of CRP then turns on the genes that help a microbe survive in a human host.
The researchers hope that once the switching mechanism is understood the data can be used to develop new methods for preventing tuberculosis and other pathogenic bacterial diseases.