IN DRUG DESIGN, A LOOSE FIT MAY BE BEST BET

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U.S. Department of Health and Human Services 
NATIONAL INSTITUTES OF HEALTH 
NIH News 
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
http://www.niddk.nih.gov/
National Institute on Deafness and Other Communication Disorders (NIDCD)

http://www.nidcd.nih.gov/

FOR IMMEDIATE RELEASE: Friday, May 12, 2006

CONTACT: Marcia Vital (NIDDK), 301-496-3583, niddkmedia@xxxxxxxxxxxx;
Jennifer Wenger (NIDCD), 301-496-7243, jwenger@xxxxxxxxxxxx

IN DRUG DESIGN, A LOOSE FIT MAY BE BEST BET

Chemical knockoffs resembling a key thyroid-related hormone are, in
certain cases, more effective than the real thing at activating the
target receptor, says a new study conducted in part by researchers at
the National Institute of Diabetes and Digestive and Kidney Diseases
(NIDDK) and the National Institute on Deafness and Other Communication
Disorders (NIDCD), two of the National Institutes of Health (NIH). The
improved performance is related to how closely couple the chemical and
receptor are, the scientists conclude, with a loose connection being
more effective than a tight one. The findings are at odds with the
widely held notion that the stronger the association between a hormone
and its receptor, the more effective its cellular signaling. If the
findings hold true for similar hormone-receptor reactions, they could
help change the way that drug therapies are designed for a host of
health problems, from smell and taste disorders to heart disease,
asthma, migraine, and pain. The study is published in the May 12, 2006,
issue of the "Journal of Biological Chemistry".

The researchers looked at thyrotropin-releasing hormone, or TRH, a
hormone released in the brain that kicks off a chain of events
throughout the body, including the stimulation of the thyroid gland. As
with many of the body's hormones, cells recognize TRH using a receptor
belonging to a mega-family of proteins known as G-protein-coupled
receptors (GPCRs), which play a lead role in cell-to-cell communication.
When a hormone binds to its designated GPCR on the outside of a cell, a
specific G-protein is activated within the cell, initiating a cascade of
biochemical events leading to the unique and appropriate cellular
response to that hormone.

"GPCRs are the targets of roughly a third of medicines sold today, so if
this finding for TRH holds for other GPCR targets, it could have
significant implications for drug development," says Marvin C.
Gershengorn, M.D., director of NIDDK's Division of Intramural Research
and senior author of the paper.

"At first glance, a cellular process that affects the thyroid gland may
not seem especially meaningful to the study of communication disorders,"
says John Northup, Ph.D., who heads the Section on Signal Transduction
of NIDCD's Laboratory of Cellular Biology. "However this research
provides information that is fundamental to cellular signaling, a
function that is essential to all cells in all systems in the body,
including our sensory systems of hearing, balance, taste, and smell."

By tweaking portions of the TRH molecule, the researchers developed six
slightly edited versions, while retaining most of the properties of the
natural hormone. Measuring the cellular response when hormone meets
receptor, they found that the lower the affinity between the two, the
stronger the signal that is elicited, with certain analogs performing up
to twice as effectively as TRH. As to why this would be the case, the
researchers suggest that a loose connection between hormone and GPCR may
allow a hormone to repetitively dock to and undock from its associated
GPCR, activating a succession of G-proteins, and firing signal after
signal. A tight connection, alternatively, may tie up a hormone with its
GPCR, activating one G-protein, and limiting its signaling ability.

In future studies, the scientists hope to determine whether their
findings are consistent with other hormone-GPCR reactions. Other
researchers taking part in the study represent the National Institute of
Pharmaceutical Education and Research, Punjab, India.

NIDDK, part of the National Institutes of Health (NIH), conducts and
supports research on diabetes; endocrine and metabolic diseases;
digestive diseases, nutrition, and obesity; and kidney, urologic and
hematologic diseases. Spanning the full spectrum of medicine and
afflicting people of all ages and ethnic groups, these diseases
encompass some of the most common, severe, and disabling conditions
affecting Americans. For more information about NIDDK programs, see the
Web site at www.niddk.nih.gov.

NIDCD supports and conducts research and research training on the normal
and disordered processes of hearing, balance, smell, taste, voice,
speech and language and provides health information, based upon
scientific discovery, to the public. For more information about NIDCD
programs, see the Web site at www.nidcd.nih.gov.

The National Institutes of Health (NIH) -- "The Nation's Medical
Research Agency" -- includes 27 Institutes and Centers and is a
component of the U.S. Department of Health and Human Services. It is the
primary federal agency for conducting and supporting basic, clinical and
translational medical research, and it investigates the causes,
treatments, and cures for both common and rare diseases. For more
information about NIH and its programs, visit www.nih.gov.
  
##
 
This NIH News Release is available online at:
http://www.nih.gov/news/pr/may2006/niddk-12.htm.

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