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HTS Assays for Targeting the cGAS STING Pathway in Autoimmune Diseases and Cancer
Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R43GM123833-01
Agency Tracking Number: R43GM123833
Amount:
$288,683.00
Phase:
Phase I
Program:
SBIR
Solicitation Topic Code:
300
Solicitation Number:
PA16-302
Timeline
Solicitation Year:
2016
Award Year:
2017
Award Start Date (Proposal Award Date):
2017-05-01
Award End Date (Contract End Date):
2018-04-30
Small Business Information
5500 NOBEL DR STE 230, Madison, WI, 53711-4951
DUNS:
119165251
HUBZone Owned:
N
Woman Owned:
N
Socially and Economically Disadvantaged:
N
Principal Investigator
Name: ROBERT LOWERY
Phone: (608) 441-2966
Email: bob.lowery@bellbrook-labs.com
Phone: (608) 441-2966
Email: bob.lowery@bellbrook-labs.com
Business Contact
Name: ROBERT LOWERY
Phone: (608) 227-4501
Email: bob.lowery@bellbrooklabs.com
Phone: (608) 227-4501
Email: bob.lowery@bellbrooklabs.com
Research Institution
N/A
Abstract
SUMMARY
Cytoplasmic nucleic acids alert the immune system to invading pathogens and trigger a robust type I interferon
IFN response via activation of the STING stimulator of interferon genes receptor The sensor for
cytoplasmic nucleic acids was recently discovered to be a cyclic GMP AMP synthase which produces a
unique cyclic dinucleotide second messenger cGAMP that serves as an agonist for the STING receptor
Aberrant activation of the cGAS STING pathway is rapidly emerging as an important underlying cause of
debilitating and sometimes fatal autoimmune disorders including systemic lupus erythematosus SLE
scleroderma and Aicardi Goutieres Syndrome AGS cGAS is an obvious target for therapeutic intervention
In addition very recent studies have indicated that stimulating the STING pathway may be an effective strategy
for cancer immunotherapy Development of small molecule inhibitors and activators of cGAS are clearly
therapeutic strategies that need to be explored However development of homogenous i e mix and read
cGAS assays for high throughput screening HTS of small molecules is quite challenging as it requires
specific detection of the cGAMP product in the presence of the substrates ATP and GTP Current assay
methods involve chromatographic isolation of radioactive cGAMP produced from radiolabeled substrates From
a broader perspective simple homogenous methods for detecting cGAMP in cell and tissue samples would be
an extremely powerful tool for basic research drug discovery and translational studies targeting the cGAS
STING pathway Our long term Phase I Phase II goal is to develop robust HTS compatible cGAS enzymatic
assays and cellular cGAMP assays to accelerate discovery and clinical translation of compounds that
modulate STING mediated immune responses
In Phase I we will develop homogenous immunodetection methods for cGAMP with fluorescence polarization
FP and time resolved F rster resonance energy transfer TR FRET signals and incorporate them into
biochemical HTS assays for cGAS BellBrook has pioneered the development of HTS assays based on
detection of nucleotides and our preliminary studies indicate that we will be successful in producing a
monoclonal antibody mAb for cGAMP with the selectivity required for a cGAS enzymatic assay We will
complete development and characterization of cGAMP mAbs synthesize fluorescent tracers that bind to the
mAbs and develop the FP and TR FRET based competitive immunoassays We will then produce
recombinant human cGAS using well defined E coli expression and affinity purification methods and optimize
the cGAS enzymatic assays Lastly we will perform pilot screens with a LOPAC library of pharmacologically
active compounds and a K diversity set to assess the level of assay interference and to demonstrate robust
HTS performance The proposed assays will fulfill the key requirements for HTS including homogenous
detection robustness good dynamic range low signal variability low levels of interference and outstanding
reagent and signal stability
In Phase II we will complete development of the biochemical cGAS HTS assay including full scale
reproducible production of stable reagents for commercial assay kits We will also develop optimize and
validate the reagents for the more challenging requirements of detecting cGAMP in cell lysates and tissue
samples i e as an endpoint in phenotypic HTS assays and translational studies in animals Development of
simple HTS homogenous methods for cGAMP in biological samples combined with cGAS enzyme assays will
provide a powerful platform for discovering and characterizing compounds that modulate STING mediated
immune responses and translating them into clinical candidates Narrative
The ability to sense foreign nucleic acids and mount an immune response is an important
weapon in the bodyandapos s armory against invading pathogens however when this system becomes
aberrantly activated by self DNA it causes debilitating autoimmune disorders such as lupus and
scleroderma We plan to develop simple rapid assays to detect a recently discovered signaling
molecule that plays a central role in the immune response to nucleic acids the assays will
enable scientists to search for drugs that prevent aberrant immune activation in autoimmune
diseases * Information listed above is at the time of submission. *