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 Applications

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.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43AG020473-01
Application #
6444843
Study Section
Special Emphasis Panel (ZRG1-BDCN-6 (10))
Program Officer
Buckholtz, Neil
Project Start
2002-07-15
Project End
2003-11-30
Budget Start
2002-07-15
Budget End
2003-11-30
Support Year
1
Fiscal Year
2002
Total Cost
$201,831
Indirect Cost
Name
Cognosci, Inc.
Department
Type
DUNS #
141881727
City
Research Triangle Park
State
NC
Country
United States
Zip Code
27709
Shvartsman, A L; Sarantseva, S V; Vitek, M P (2011) [Potential role of presenilin 1 in regulation of synaptic function]. Tsitologiia 53:959-67
Li, Feng-Qiao; Fowler, Kenneth A; Neil, Jessica E et al. (2010) An apolipoprotein E-mimetic stimulates axonal regeneration and remyelination after peripheral nerve injury. J Pharmacol Exp Ther 334:106-15
Tukhovskaya, Elena A; Yukin, Alexey Yu; Khokhlova, Oksana N et al. (2009) COG1410, a novel apolipoprotein-E mimetic, improves functional and morphological recovery in a rat model of focal brain ischemia. J Neurosci Res 87:677-82