R01AI173109
Project Grant
Overview
Grant Description
BROADLY NEUTRALIZING SARS-COV-2 PEPTIDIC KNOBS - ABSTRACT
TARGETED THERAPEUTIC AGENTS RANGE IN SIZE FROM VERY SMALL ORGANIC MOLECULES (100’S OF DA) TO PROTEIN-BASED MOLECULES LIKE MONOCLONAL ANTIBODIES (~150,000 DA).
SMALL DISULFIDE BONDED PEPTIDES HAVE EVOLVED IN MANY SPECIES, INCLUDING PLANTS AND ANIMALS, TO HAVE IDEAL PHARMACOLOGICAL PROPERTIES INCLUDING HIGH AFFINITY TARGET BINDING, STABILITY TO PROTEASES, HEAT AND OTHER STRESSES.
SUCH PEPTIDES INCLUDE “CYCLOTIDES” OR “KNOTTINS” WHICH CAN INHIBIT ENZYMES, ION CHANNELS, AND GPCRS WITH HIGH POTENCY AND ARE OFTEN THE MAJOR ACTIVE COMPONENT OF VENOMS OF MANY PREDATOR ORGANISMS.
WE HAVE UNCOVERED CONVERGENT EVOLUTION BETWEEN ULTRALONG THIRD COMPLEMENTARY DETERMINING REGIONS (CDR H3S) IN THE HEAVY CHAIN OF AN UNUSUAL CLASS OF COW ANTIBODIES AND CYCLOTIDE/KNOTTIN PEPTIDES.
WE CAN PRODUCE THESE “KNOB” PEPTIDES IN MICROBIAL SYSTEMS AND THEY RETAIN THE BINDING AND POTENCY PROPERTIES OF THE PARENT ANTIBODY.
THESE TINY PEPTIDE-BASED MOLECULES ARE SMALL (~4-6 KDA), HIGHLY STABLE, AND CAN BIND TARGETS AT SUBNANOMOLAR KD.
WE HAVE ALREADY DEVELOPED A PANEL OF VIRUS NEUTRALIZING KNOB PEPTIDES AGAINST SARS-COV-2 WHICH BIND UNIQUE EPITOPES, AND SOME OF WHICH MAINTAIN HIGH AFFINITY BINDING TO VARIOUS SARS-COV-2 VARIANTS, INCLUDING THE RECENT ‘DELTA’ AND ‘OMICRON’ STRAINS.
THE HIGH STABILITY, POTENCY, AND STRAIGHTFORWARD MANUFACTURING PATH ENABLES MULTIPLE ROUTES OF ADMINISTRATION, POTENTIALLY INCLUDING INHALED OR INTRANASAL DELIVERY, WHICH COULD BE VERY IMPORTANT PROPHYLACTIC OR TREATMENT IN THE CURRENT OR FUTURE CORONAVIRUS PANDEMIC.
OUR GOALS IN THIS PROJECT ARE TO FURTHER DEVELOP THE TECHNOLOGY TO IDENTIFY PEPTIDIC KNOB DOMAINS, EXPAND OUR PANEL OF KNOBS AGAINST SARS-COV-2 VARIANTS AND OTHER CORONAVIRUSES LIKE MERS-COV AND SARS-COV-1, UNDERSTAND THE STRUCTURAL BASIS OF THEIR BINDING, AND VALIDATE THEIR ACTIVITY IN VITRO AND IN VIVO.
THE KNOBS IDENTIFIED HERE CAN POTENTIALLY BE USED AS MONOTHERAPY OR COMBINATION THERAPY IN THE CURRENT OR A NEW CORONAVIRUS PANDEMIC, AND WILL BE A VALUABLE NEW THERAPEUTIC CLASS TO ADD TO THE ARSENAL AGAINST CORONAVIRUS DISEASE.
TARGETED THERAPEUTIC AGENTS RANGE IN SIZE FROM VERY SMALL ORGANIC MOLECULES (100’S OF DA) TO PROTEIN-BASED MOLECULES LIKE MONOCLONAL ANTIBODIES (~150,000 DA).
SMALL DISULFIDE BONDED PEPTIDES HAVE EVOLVED IN MANY SPECIES, INCLUDING PLANTS AND ANIMALS, TO HAVE IDEAL PHARMACOLOGICAL PROPERTIES INCLUDING HIGH AFFINITY TARGET BINDING, STABILITY TO PROTEASES, HEAT AND OTHER STRESSES.
SUCH PEPTIDES INCLUDE “CYCLOTIDES” OR “KNOTTINS” WHICH CAN INHIBIT ENZYMES, ION CHANNELS, AND GPCRS WITH HIGH POTENCY AND ARE OFTEN THE MAJOR ACTIVE COMPONENT OF VENOMS OF MANY PREDATOR ORGANISMS.
WE HAVE UNCOVERED CONVERGENT EVOLUTION BETWEEN ULTRALONG THIRD COMPLEMENTARY DETERMINING REGIONS (CDR H3S) IN THE HEAVY CHAIN OF AN UNUSUAL CLASS OF COW ANTIBODIES AND CYCLOTIDE/KNOTTIN PEPTIDES.
WE CAN PRODUCE THESE “KNOB” PEPTIDES IN MICROBIAL SYSTEMS AND THEY RETAIN THE BINDING AND POTENCY PROPERTIES OF THE PARENT ANTIBODY.
THESE TINY PEPTIDE-BASED MOLECULES ARE SMALL (~4-6 KDA), HIGHLY STABLE, AND CAN BIND TARGETS AT SUBNANOMOLAR KD.
WE HAVE ALREADY DEVELOPED A PANEL OF VIRUS NEUTRALIZING KNOB PEPTIDES AGAINST SARS-COV-2 WHICH BIND UNIQUE EPITOPES, AND SOME OF WHICH MAINTAIN HIGH AFFINITY BINDING TO VARIOUS SARS-COV-2 VARIANTS, INCLUDING THE RECENT ‘DELTA’ AND ‘OMICRON’ STRAINS.
THE HIGH STABILITY, POTENCY, AND STRAIGHTFORWARD MANUFACTURING PATH ENABLES MULTIPLE ROUTES OF ADMINISTRATION, POTENTIALLY INCLUDING INHALED OR INTRANASAL DELIVERY, WHICH COULD BE VERY IMPORTANT PROPHYLACTIC OR TREATMENT IN THE CURRENT OR FUTURE CORONAVIRUS PANDEMIC.
OUR GOALS IN THIS PROJECT ARE TO FURTHER DEVELOP THE TECHNOLOGY TO IDENTIFY PEPTIDIC KNOB DOMAINS, EXPAND OUR PANEL OF KNOBS AGAINST SARS-COV-2 VARIANTS AND OTHER CORONAVIRUSES LIKE MERS-COV AND SARS-COV-1, UNDERSTAND THE STRUCTURAL BASIS OF THEIR BINDING, AND VALIDATE THEIR ACTIVITY IN VITRO AND IN VIVO.
THE KNOBS IDENTIFIED HERE CAN POTENTIALLY BE USED AS MONOTHERAPY OR COMBINATION THERAPY IN THE CURRENT OR A NEW CORONAVIRUS PANDEMIC, AND WILL BE A VALUABLE NEW THERAPEUTIC CLASS TO ADD TO THE ARSENAL AGAINST CORONAVIRUS DISEASE.
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
San Diego,
California
921271752
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 286% from $967,225 to $3,730,300.
Applied Biomedical Science Institute was awarded
Advanced Peptide-Based Therapeutics for Targeted COVID-19 Treatment
Project Grant R01AI173109
worth $3,730,300
from the National Institute of Allergy and Infectious Diseases in June 2023 with work to be completed primarily in San Diego California United States.
The grant
has a duration of 5 years and
was awarded through assistance program 93.855 Allergy and Infectious Diseases Research.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 6/5/26
Period of Performance
6/9/23
Start Date
5/31/28
End Date
Funding Split
$3.7M
Federal Obligation
$0.0
Non-Federal Obligation
$3.7M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01AI173109
Additional Detail
Award ID FAIN
R01AI173109
SAI Number
R01AI173109-2926069784
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Nonprofit With 501(c)(3) IRS Status (Other Than An Institution Of Higher Education)
Awarding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Funding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Awardee UEI
K6YFV76PCGB7
Awardee CAGE
85ZM0
Performance District
CA-50
Senators
Dianne Feinstein
Alejandro Padilla
Alejandro Padilla
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Institute of Allergy and Infectious Diseases, National Institutes of Health, Health and Human Services (075-0885) | Health research and training | Grants, subsidies, and contributions (41.0) | $967,225 | 100% |
Modified: 6/5/26