Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Feb 26;63(9):e202309958.
doi: 10.1002/anie.202309958. Epub 2023 Nov 22.

Exploring Peptido-Nanocomposites in the Context of Amyloid Diseases

Affiliations
Review

Exploring Peptido-Nanocomposites in the Context of Amyloid Diseases

Nicholas Andrikopoulos et al. Angew Chem Int Ed Engl. .

Abstract

Therapeutic peptides are a major class of pharmaceutical drugs owing to their target-binding specificity as well as their versatility in inhibiting aberrant protein-protein interactions associated with human pathologies. Within the realm of amyloid diseases, the use of peptides and peptidomimetics tailor-designed to overcome amyloidogenesis has been an active research endeavor since the late 90s. In more recent years, incorporating nanoparticles for enhancing the biocirculation and delivery of peptide drugs has emerged as a frontier in nanomedicine, and nanoparticles have further demonstrated a potency against amyloid aggregation and cellular inflammation to rival strategies employing small molecules, peptides, and antibodies. Despite these efforts, however, a fundamental understanding of the chemistry, characteristics and function of peptido-nanocomposites is lacking, and a systematic analysis of such strategy for combating a range of amyloid pathogeneses is missing. Here we review the history, principles and evolving chemistry of constructing peptido-nanocomposites from bottom up and discuss their future application against amyloid diseases that debilitate a significant portion of the global population.

Keywords: Amyloid Disease; Amyloidosis; Nanoparticle; Peptide; Peptidomimetic.

PubMed Disclaimer

References

    1. T. P. Knowles, M. Vendruscolo, C. M. Dobson, Nat. Rev. Mol. Cell Biol. 2014, 15, 384-396.
    1. E. D. Eanes, G. G. Glenner, J. Histochem. Cytochem. 1968, 16, 673-677.
    1. P. C. Ke, R. Zhou, L. C. Serpell, R. Riek, T. P. J. Knowles, H. A. Lashuel, E. Gazit, I. W. Hamley, T. P. Davis, M. Fandrich, D. E. Otzen, M. R. Chapman, C. M. Dobson, D. S. Eisenberg, R. Mezzenga, Chem. Soc. Rev. 2020, 49, 5473-5509.
    1. P. C. Ke, M. A. Sani, F. Ding, A. Kakinen, I. Javed, F. Separovic, T. P. Davis, R. Mezzenga, Chem. Soc. Rev. 2017, 46, 6492-6531.
    1. D. Balchin, M. Hayer-Hartl, F. U. Hartl, Science 2016, 353, aac4354.

Publication types

LinkOut - more resources