General 'Control
Switch' for Protein Activity
Our bodies could not maintain their
existence without thousands of proteins performing myriad
vital tasks within cells. Since malfunctioning proteins
can cause disease, the study of protein structure and
function can lead to the development of drugs and treatments
for numerous disorders.
For example, the discovery
of insulin's role in diabetes paved the way for the
development of a treatment based on insulin injections.
Yet, despite enormous research efforts led by scientists
worldwide, the cellular function of numerous proteins
is still unknown. To reveal this function, scientists
perform various genetic manipulations to increase or,
conversely, decrease the production of a certain protein,
but existing manipulations of this sort are complicated
and do not fully meet the researchers' needs.
Prof. Mordechai "Moti" Liscovitch and graduate
student Oran Erster of the Weizmann Institute's Biological
Regulation Department, together with Dr. Miri Eisenstein
of Chemical Research Support, have recently developed
a unique "switch" that can control the activity
of any protein, raising it several-fold or stopping
it almost completely. The method provides researchers
with a simple and effective tool for exploring the function
of unknown proteins, and in the future the new technique
may find many additional uses.
The switch has a genetic component and a chemical component:
Using genetic engineering, the scientists insert a short
segment of amino acids into the amino acid sequence
making up the protein. This segment is capable of binding
strongly and selectively to a particular chemical drug,
which affects the activity level of the engineered protein
by increasing or reducing it. When the drug is no longer
applied, or when it is removed from the system, the
protein returns to its natural activity level.
As reported recently in the journal Nature Methods,
the first stage of the method consists of preparing
a set of genetically engineered proteins (called a "library"
in scientific language) with the amino acid segment
inserted in different places. In the second stage, the
engineered proteins are screened to identify the ones
that respond to the drug in a desired manner. The researchers
have discovered that in some of the engineered proteins
the drug increased the activity level, while in others
this activity was reduced. Says Prof. Liscovitch: "We
were surprised by the effectiveness of the method --
it turns out that a small set of engineered proteins
is needed to find the ones that respond to the drug.
With their greater resources, biotechnology companies
will be able to create much larger sets of engineered
proteins in order to find one that best meets their
needs."
The method developed by the Weizmann Institute scientists
is ready for immediate use, both in basic biomedical
research and in the pharmaceutical industry, in the
search for proteins that can serve as targets for new
drugs. Beyond offering a potent tool that can be applied
to any protein, the method has an important advantage
compared with other techniques: It allows the total
and precise control over the activity of an engineered
protein. Such activity can be brought to a desired level
or returned to its natural level, at specific locations
in the body and at specific times -- all this by giving
exact and well-timed doses of the same simple drug.
In addition, the method could be used one day in gene
therapy. It may be possible to replace damaged proteins
that cause severe diseases with genetically engineered
proteins, and to control these proteins' activity levels
in a precise manner by giving appropriate doses of the
drug. Another potential future application is in agricultural
genetic engineering.
The method might make it possible, for example, to create
genetically engineered plants in which the precise timing
of fruit ripening would be controlled using a substance
that increases the activity of proteins responsible
for ripening. Moreover, numerous proteins are used in
industrial processes, as biological sensors and in other
applications. The possibility of controlling these applications
-- strengthening or slowing the rate of protein activity
in an immediate and reversible manner -- can be of great
value.
Source: Invention
Intelligence, July - August 2007