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@ARTICLE{LaRosa:874630,
author = {La Rosa, Carmelo and Condorelli, Marcello and Compagnini,
Giuseppe and Lolicato, Fabio and Milardi, Danilo and Do,
Trang Nhu and Karttunen, Mikko and Pannuzzo, Martina and
Ramamoorthy, Ayyalusamy and Fraternali, Franca and Collu,
Francesca and Rezaei, Human and Strodel, Birgit and Raudino,
Antonio},
title = {{S}ymmetry-breaking transitions in the early steps of
protein self-assembly},
journal = {European biophysics journal},
volume = {49},
number = {2},
issn = {1432-1017},
address = {New York},
publisher = {Springer},
reportid = {FZJ-2020-01550},
pages = {175 - 191},
year = {2020},
abstract = {Protein misfolding and subsequent self-association are
complex, intertwined processes, resulting in development of
a het-erogeneous population of aggregates closely related to
many chronic pathological conditions including Type 2
Diabetes Mellitus and Alzheimer’s disease. To address this
issue, here, we develop a theoretical model in the general
framework of linear stability analysis. According to this
model, self-assemblies of peptides with pronounced
conformational flexibility may become, under particular
conditions, unstable and spontaneously evolve toward an
alternating array of partially ordered and disordered
monomers. The predictions of the theory were verified by
atomistic molecular dynamics (MD) simulations of islet
amyloid polypeptide (IAPP) used as a paradigm of
aggregation-prone polypeptides (proteins). Simulations of
dimeric, tetrameric, and hexameric human-IAPP
self-assemblies at physiological electrolyte concentration
reveal an alternating dis-tribution of the smallest domains
(of the order of the peptide mean length) formed by
partially ordered (mainly β-strands) and disordered (turns
and coil) arrays. Periodicity disappears upon weakening of
the inter-peptide binding, a result in line with the
predictions of the theory. To further probe the general
validity of our hypothesis, we extended the simulations to
other peptides, the Aβ(1–40) amyloid peptide, and the
ovine prion peptide as well as to other proteins (SOD1
dimer) that do not belong to the broad class of
intrinsically disordered proteins. In all cases, the
oligomeric aggregates show an alternate distribution of
partially ordered and disordered monomers. We also carried
out Surface Enhanced Raman Scattering (SERS) measurements of
hIAPP as an experimental validation of both the theory and
in silico simulations},
cin = {IBI-7},
ddc = {570},
cid = {I:(DE-Juel1)IBI-7-20200312},
pnm = {551 - Functional Macromolecules and Complexes (POF3-551)},
pid = {G:(DE-HGF)POF3-551},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32123956},
UT = {WOS:000517713400001},
doi = {10.1007/s00249-020-01424-1},
url = {https://juser.fz-juelich.de/record/874630},
}