4.8 Article

Supramolecular Copolymers of Peptides and Lipidated Peptides and Their Therapeutic Potential

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 144, 期 12, 页码 5562-5574

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.2c00433

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资金

  1. Center for Regenerative Nanomedicine at the Simpson Querrey Institute for BioNanotechnology
  2. U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0020884]
  3. Paralyzed Veterans of America (PVA) Research Foundation fellowship [PVA17RF0008]
  4. Research Foundation Flanders (FWO) Postdoctoral Mandates [12G2718N]
  5. KU Leuven [JUMO-15-0514]
  6. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF) [ECCS-2025633]
  7. Robert H. Lurie Comprehensive Cancer Center of Northwestern University
  8. NCI Cancer Center Support grant [P30 CA060553]
  9. SHyNE Resource (NSF) [ECCS-2025633, NSF ECCS-2025633]
  10. NIH [1S10OD012016-01/1S10RR019071-01A1, NSF DMR-1720139]
  11. NCI CCSG [P30 CA060553]
  12. Robert H Lurie Comprehensive Cancer Center
  13. Northwestern University
  14. Dow Chemical Company
  15. DuPont de Nemours, Inc.
  16. DOE Office of Science
  17. Argonne National Laboratory [DE-AC02-06CH11357]
  18. National Science Foundation [0960140]
  19. Office of the Provost
  20. Office for Research
  21. Northwestern University Information Technology
  22. U.S. Department of Energy (DOE) [DE-SC0020884] Funding Source: U.S. Department of Energy (DOE)

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Supramolecular peptide chemistry provides a versatile strategy for creating new biomaterials that can deliver various peptide therapeutics or integrate other types of bioactivity. This study focuses on the co-assembly of lipidated beta-sheet-forming peptides with soluble short peptides, resulting in supramolecular copolymers with different degrees of internal order. The copolymers exhibit thermodynamic metastability, leading to the spontaneous release of peptide monomers, which could serve as a potential mechanism for drug delivery.
Supramolecular peptide chemistry offers a versatile strategy to create chemical systems useful as new biomaterials with potential to deliver nearly 1000 known candidate peptide therapeutics or integrate other types of bioactivity. We report here on the co-assembly of lipidated beta-sheet-forming peptides with soluble short peptides, yielding supramolecular copolymers with various degrees of internal order. At low peptide concentrations, the co-monomer is protected by lodging within internal aqueous compartments and stabilizing internal beta-sheets formed by the lipidated peptides. At higher concentrations, the peptide copolymerizes with the lipidated peptide and disrupts the beta-sheet secondary structure. The thermodynamic metastability of the coassembly in turn leads to the spontaneous release of peptide monomers and thus serves as a potential mechanism for drug delivery. We demonstrated the function of these supramolecular systems using a drug candidate for Alzheimer's disease and found that the copolymers enhance neuronal cell viability when the soluble peptide is released from the assemblies.

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