[Federal Register Volume 70, Number 38 (Monday, February 28, 2005)]
[Notices]
[Pages 9659-9660]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 05-3830]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions; Availability for Licensing
AGENCY: National Institutes of Health, Public Health Service, DHHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The inventions listed below are owned by an agency of the U.S.
Government and are available for licensing in the U.S. in accordance
with 35 U.S.C. 207 to achieve expeditious commercialization of results
of federally-funded research and development. Foreign patent
applications are filed on selected inventions to extend market coverage
for companies and may also be available for licensing.
ADDRESSES: Licensing information and copies of the U.S. patent
applications listed below may be obtained by writing to the indicated
licensing contact at the Office of Technology Transfer, National
Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville,
Maryland 20852-3804; telephone: 301/496-7057; fax: 301/402-0220. A
signed Confidential Disclosure Agreement will be required to receive
copies of the patent applications.
Compositions and Methods for the Treatment of Immune-Related Disease
F. Xavier Valencia and Peter E. Lipsky (NIAMS), U.S. Provisional
Application filed 07 Jan 2005 (DHHS Reference No. E-355-2004/0-US-01).
Licensing Contact: Fatima Sayyid; 301/435-4521;
[email protected].
The ability of the immune system to discriminate between self and
non-self is controlled by central and peripheral tolerance mechanisms.
One of the most important ways the immune system controls the outcome
of such a response is through naturally occurring CD4+CD25+ regulatory
T cells.
The present invention relates to compositions and methods for
treating immune related disease, a method for determining the presence
of or predisposition to an immune related disease, and a pharmaceutical
composition for treating an immune related disease in a mammal.
In addition to licensing, the technology is available for further
development through collaborative research opportunities with the
inventors.
Expression Tags for High Yield Soluble Expression of Recombinant
Proteins
Deb K. Chatterjee and Dominic Esposito (NCI), U.S. Provisional
Application No. 60/564,982 filed 26 Apr 2004 (DHHS Reference No. E-103-
2004/0-US-01).
Licensing Contact: Susan Carson, 301-435-5020;
[email protected].
Production of large quantities of soluble and correctly folded
proteins is essential for a variety of applications ranging from
functional analysis and structure determination to clinical trials. E.
coli is a widely used expression system that offers the advantages of
ease of handling, cost-effectiveness and the ability to produce
proteins in high yield. However, the enhanced production obtainable
with E. coli expression systems is frequently accompanied by problems
of protein insolubility, production host non-viability and aberrant
protein folding. Many strategies have been proposed to address these
problems, in particular the use of fusion vectors that mediate the
expression of a target gene linked to a peptide signal sequence or to a
``chaperone'' or ``carrier'' protein that is capable of ``escorting''
the fusion protein out of the cytoplasm and into the periplasmic space.
However, there remains a need for methods that provide soluble proteins
that are correctly folded and in functional form without unacceptably
diminishing the yield of recovered protein or requiring complex host
strains.
NIH researchers have developed a fusion polynucleotide in which a
polynucleotide encoding a desired target protein is linked to one or
more chaperone protein domains (Skp and DsbC) with or without the
signal sequence. This permits the expressed proteins to be transported
to the periplasm or to be retained in the cytoplasm respectively and
these vectors were used to successfully express significant amounts of
such difficult to express proteins as Hif1a, Folliculin (fol), a
Folliculin domain (FD), Wnt5a, Endostatin, YopD, IL13 and IFN-Hybrid3.
These fusion vectors are available for licensing and are useful tools
for the expression of commercially viable amounts of functional
proteins of therapeutic and scientific interest.
In addition to licensing, the technology is available for further
development through collaborative research with the inventors via a
Cooperative Research and Development Agreement (CRADA).
Novel Potent Monoamine Oxidase Inhibitors
Kenneth L. Kirk et al. (NIDDK), U.S. Provisional Application No.
60/484,710 filed 03 Jul 2003 (DHHS Reference No. E-226-2003/0-US-01);
PCT Application No. PCT/US04/21505 filed 01 Jul 2004 (DHHS Reference
No. E-226-2003/0-PCT-02).
Licensing Contact: Norbert Pontzer; 301/435-5502;
[email protected].
Copper- (EC, 1.4.3.6) and flavin-containing amine oxidases (EC,
1.4.3.4) make up two general classes of the widely distributed
monoamine oxidases. Reversible and irreversible inhibitors of the
flavin monoamine oxidases have been developed and investigated for
treatment of diseases of the CNS such as depression, Parkinson's
disease and Alzheimer's disease. These researchers have developed
several new arylethyl and benzyl amine derivatives that incorporate
both the key cyclopropane ring and fluorine substitution at strategic
positions. The combined effects of this substitution pattern have led
to new inhibitors of greatly increased potency and selectivity for all
classes of monoamine oxidases. Their potent copper amine oxidase
inhibitors are the best reversible inhibitors known and could provide
vascular protection in advanced diabetics. Further information on these
compounds can be found in Yoshida et al., J. Med. Chem. (25 Mar 2004)
47 (7): 1796-1806, 2004, and Yoshida et al.,
[[Page 9660]]
Bioorg. Med. Chem. (15 May 2004) 12 (10): 2645-2652.
Dated: February 17, 2005.
Steven M. Ferguson,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
[FR Doc. 05-3830 Filed 2-25-05; 8:45 am]
BILLING CODE 4140-01-P