SBIR/STTR Research Award

Next-generation ligandomics technology to globally map cellular ligands of the retina

Award identifier 2f14700a6583f79937f8f4c1ef8a14e989ec41b7f1c63654c6f6e0b3b808e426Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$226,255

Program and phase

SBIR · Phase I

Award year

2020

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
LIGANDOMICSRX LLC
Proposal award date
2020-09-01
Contract end date
2021-08-31
UEI
M433VMAUAXQ5
Solicitation number
PA17-147
Topic code
N

Research abstract

Project Summary Extracellular ligands are among the most valuable drug targets, but are much less exploited for disease therapy than plasma membrane receptors. This is mainly because the technical hurdles for ligand discovery are much greater than those for receptors, the latter of which can be conveniently identified based on their transmembrane domains. Current omics technologies, such as proteomics, functional proteomics and transcriptomics, are not designed to map extracellular ligands. Consequently, extracellular ligands are traditionally identified and characterized on a case-by-case basis with inherent technical challenges. It is even more daunting to delineate ligands with therapeutic potential. To address these challenges, we recently developed a unique platform technology of ligandomics for global mapping of cell-wide ligands as well as disease-selective ligands in the absence of receptor information. The validity and utility of this innovative technology has been demonstrated by efficient discovery of highly disease-selective angiogenic factors and rapid development of novel anti-angiogenic therapies with high efficacy and minimal side effects on normal vessels. However, this first-generation ligandomics technology has the limited application only to homogeneous cells. In this project, we will develop next-generation ligandomics technology that is applicable to any type of cells. In Aim 1, we will develop the next- generation ligandomics technology to map ligand-secreting and binding cells connected through different ligand signaling pathways. In Aim 2, we will apply the new technology to diabetic and healthy retina to systematically identify diabetes-selective cellular ligands. The successful implementation of this project will markedly improve the capacity of ligandomics to identify cellular ligands and disease-selective ligands for different cells. Our new ligandomics technology developed in this project is universally applicable to any cells, tissues and diseases, and therefore may have the potential to impact on a broad field of cell biology research and drug target discovery.Project Narrative Cellular ligands are among the most valuable therapeutic targets but are traditionally identified on a case-by- case basis with technical challenges. This project is to develop a new technology for global mapping of extracellular ligands for heterogeneous cells. The new technology can also systematically identify disease- selective ligands as high-quality targets to develop novel drugs.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.