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A new strategy to reconcile amyloid cross-seeding and amyloid prevention in a binary system of α-synuclein fragmental peptide and hIAPP.

Abstract
Amyloid cross-seeding and amyloid inhibition are two different research subjects being studied separately for different pathological purposes, in which amyloid cross-seeding targets to study the co-aggregation of different amyloid proteins and potential molecular links between different neurodegenerative diseases, while amyloid inhibition aims to design different molecules for preventing amyloid aggregation. While both amyloid cross-seeding and amyloid inhibition are critical for better understanding the pathological causes of different neurodegenerative diseases including Parkinson disease (PD) and Type 2 diabetes (T2D), less efforts have been made to reconcile the two phenomena. Herein, we proposed a new preventive strategy to demonstrate (a) the cross-seeding of octapeptide TKEQVTNV from α-synuclein (associated with PD) with hIAPP (associated with T2D) and (b) the cross-seeding-promoted hIAPP fibrillization and cross-seeding-reduced hIAPP toxicity. Collective results confirmed that TKEQVTNV can indeed cross-seed with hIAPP monomers and oligomers, not protofibrils, to form β-structure-rich fibrils and to accelerate hIAPP fibrillization. Moreover, such cross-seeding-induced promotion effect by TKEQVTNV also rescued the pancreatic cells from hIAPP-induced cytotoxicity by increasing cell viability and reducing cell apoptosis simultaneously. This work provides a new angle to discover amyloid fragments and use them as amyloid modulators (inhibitors or promotors) to interfere with amyloid aggregation of other amyloid proteins, as well as sequence/structure basis to explore the amyloid cross-seeding between different amyloid proteins that may help explain a potential molecular talk between different neurodegenerative diseases.
AuthorsYijing Tang, Dong Zhang, Yonglan Liu, Yanxian Zhang, Yifan Zhou, Yung Chang, Bowen Zheng, Alice Xu, Jie Zheng
JournalProtein science : a publication of the Protein Society (Protein Sci) Vol. 31 Issue 2 Pg. 485-497 (02 2022) ISSN: 1469-896X [Electronic] United States
PMID34850985 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Copyright© 2021 The Protein Society.
Chemical References
  • Amyloid
  • Amyloid beta-Peptides
  • Amyloidogenic Proteins
  • Islet Amyloid Polypeptide
  • alpha-Synuclein
Topics
  • Amyloid (chemistry)
  • Amyloid beta-Peptides (chemistry)
  • Amyloidogenic Proteins (chemistry)
  • Humans
  • Islet Amyloid Polypeptide (chemistry)
  • Neurodegenerative Diseases
  • alpha-Synuclein (chemistry)

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