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Title: Peptides having reduced toxicity that stimulate cholesterol efflux

Patent ·
OSTI ID:1840354

The present invention provides a family of non-naturally occurring polypeptides having cholesterol efflux activity that parallels that of full-length apolipoproteins (e.g., Apo AI and Apo E), and having high selectivity for ABCA1 that parallels that of full-length apolipoproteins. Further, the peptides of the invention have little or no toxicity when administered at therapeutic and higher doses. The invention also provides compositions comprising such polypeptides, methods of identifying, screening and synthesizing such polypeptides, and methods of treating, preventing or diagnosing diseases and disorders associated with dyslipidemia, hypercholesterolemia, or inflammation; or diseases involving abnormal glucose metabolism, e.g., diabetes, metabolic syndrome; or Alzheimers Disease or frontotemporal dementia.

Research Organization:
Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE; National Institutes of Health (NIH)
DOE Contract Number:
AC02-05CH11231; HL085791
Assignee:
The Regents of the University of California (Oakland, CA)
Patent Number(s):
11,091,529
Application Number:
15/511,623
OSTI ID:
1840354
Resource Relation:
Patent File Date: 09/14/2015
Country of Publication:
United States
Language:
English

References (5)

Prevention and treatment of restenosis by local administration of drug patent February 2012
Peptides Having Reduced Toxicity Thar Stimulate Cholesterol Efflux patent-application September 2014
Peptide mediators of cholesterol efflux patent April 2013
Helical synthetic peptides that stimulate cellular cholesterol efflux patent-application September 2005
Potent and Selective Mediators of Cholesterol Efflux patent-application December 2012