SBIR/STTR Research Award

NEUROPROTECTIVE APOLIPOPROTEIN-E ANALOGS

Award identifier eb4b0fa1d2facb7682a66364fd8b692d9c6cee592bf66c9d15441972724737baAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$201,831

Program and phase

SBIR · Phase I

Award year

2002

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
COGNOSCI INC
Proposal award date
Not reported
Contract end date
Not reported
UEI
NZW4KLUZ17G3
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Apolipoprotein E (apoE) is a 299 amino acid protein that plays a palliative role in the CNS response to acute and chronic injury. We have recently demonstrated that the addition of exogenous apoE, or peptides derived from its receptor-binding domain, can reduce endogenous CNS inflammatory response. As a 20mer, this peptido-apoE-mimetic appears to act as an agonist on the LRP receptor (Low Density Lipoprotein receptor-related protein) and could have beneficial effects in whole animal models and ultimately, in human patients. Although modifications of this peptide may improve neuroprotective activity, our ultimate goal is to create a non-peptido-mimetic of apoE?s activity. Thus, in PHASE 1 of this proposal, we propose to extensively modify this lead compound, i.e. the 20 amino acid peptido-apoE-mimetic, to more precisely define its minimal and essential residues that retain binding and biological activities. In PHASE 2 of this proposal, we will make use of this SAR data (Structure-Activity Relationship) to learn how to define the space that this peptide occupies in the LRP receptor and then use this information to direct the synthesis of non-peptide molecules that can similarly act as LRP agonists in cell-based and animal-based model systems. PROPOSED COMMERCIAL APPLICATION: Following brain injury that results from stroke and closed head injury, peptides and/or compounds that protect neurons from dying would be of clinical and therapeutic benefit to the patient. Based on the demonstrated involvement of apolipoprotein-E in human brain injury, we are developing novel apoE-mimetics that help protect against neuronal death in human brain injury.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Research funding history

34 SBIR/STTR records share this UEI (2002–2015). Reported award amounts total $13,693,533. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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