In everyday life, the global positioning system (GPS) can be employed to
reliably determine the momentary location of one en route to the
desired destination. Scientists from the Institute of Physical and
Theoretical Chemistry of the University of Bonn have now developed a
molecular "GPS" with which the whereabouts of metal ions in enzymes can
be reliably determined. Such ions play important roles in all corners of
metabolism and synthesis for biological products. The "molecular GPS"
is now being featured in the journal Angewandte Chemie.
There would be no life on our planet without enzymes. These
molecules, control and enable biochemical reactions ranging from
digestion to the duplication of genetic information. "Enzymes are
spatially complex structures which can have multiple folds, sheets and
loops," says Prof. Dr. Olav Schiemann from the Institute for Physical
and Theoretical Chemistry of the University of Bonn. In the reaction
center of such a "protein knot," which is known as the "active center,"
is often one or more metal ions. This means that the substance which is
to be changed by a chemical reaction attaches to or close to the metal
ion. The ion facilitates the breakage or reformation of one or more
bonds in the attached substance and the conversion into a new substance
arises through the enzyme. Such conversions take place constantly in our
stomach, for example, where food is broken down into substances which
our body can easily absorb.
Scientists are examining how such essential enzymes work. To do this,
they must precisely know how the individual atoms are arranged in these
biomolecules. "When we know the whereabouts of the metal ion in an
enzyme, we can better understand exactly how the reactions proceed,"
says Prof. Schiemann. His working group has now determined the position
of the active center in an enzyme using a novel method which is
reminiscent in principle of the global positioning system (GPS) with
which automobile navigation systems work.
Like the maze of traffic during rush hour
"The structure of enzymes is frequently, at first glance, just as
confusing as the maze of traffic during rush hour," chuckles the
physical chemist from the University of Bonn. Similarly to how an
individual car is nearly impossible to make out in a large amount of
traffic, the metal ion "hides" in the numerous coils and folds of the
enzyme. Nonetheless, the position of the vehicle -- and also that of the
metal ion -- can be reliably determined with GPS. Several satellites
orbit our planet and indicate through the transit time of signals the
distance to a certain point on the earth, for example, a car. The site
where the distance spheres of the various satellites intersect is where
the car to be located.
The "satellites" consist of the spin labeled amino acid cysteine
The physical chemists from the University of Bonn proceeded
similarly. "Our satellites are spin labels," explains doctoral student
Dinar Abdullin. These are small organic molecules which have an unpaired
electron and which are stable. The researchers distributed six of these
"molecular satellites" in their enzyme model "azurine" -- a blue
protein with a copper ion in the center. Using computer programs, the
scientists first tracked the "orbits" of the tiny satellites in the
coils of the enzyme. They then determined the distance between the
satellites and the metal ion using a spectroscopic method, namely
PELDOR, which acts like a ruler on a molecular level. "Similar to the
GPS, we were able to precisely determine the position of the active
center in the enzyme from this," says Abdullin.
The tool kit of physical chemistry has now gained an elegant
additional method. "We developed the method for basic research but it
can also be used to clarify the structure of other enzymes," says Prof.
Schiemann. A better understanding of substance conversions at active
centers is ultimately also the foundation, for example, for industrial
drug manufacturing.
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