Evidence map›Paper›PMID 40717488›Full record

ArticleACS nano2025

Controlling Amyloid Assembly Dynamics Using Spin Interfaces.

Yael Kapon, Dror Merhav, Gal Finkelstein-Zuta, Omer Blumen, Naomi Melamed-Book, Yael Levi-Kalisman, Ilya Torchinsky, Shira Yochelis, Daniel Sharon, Lech Tomasz Baczewski and 2 more

Abstract read
In one paragraph

Article in ACS nano, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yael KaponInstitute of Applied Physics, The Hebrew University, Jerusalem 9190401, Israel.ORCID 0000-0001-5019-2117
Dror MerhavInstitute of Applied Physics, The Hebrew University, Jerusalem 9190401, Israel.ORCID 0009-0003-6775-6507
Gal Finkelstein-ZutaThe Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 6997801, Israel.ORCID 0009-0002-5708-1692
Omer BlumenInstitute of Chemistry, Hebrew University of Jerusalem, Jerusalem 91904, Israel.ORCID 0009-0009-3463-7513
Naomi Melamed-BookBio-Imaging Unit, The Alexander Silberman Institute of Life Science, The Hebrew University, Jerusalem 9190401, Israel.ORCID 0000-0001-9528-5026
Yael Levi-KalismanThe Harvey M. Krueger Family Center for Nanoscience and Nanotechnology, The Hebrew University, Jerusalem 9190401, Israel.ORCID 0000-0002-2764-2738
Ilya TorchinskyThe Harvey M. Krueger Family Center for Nanoscience and Nanotechnology, The Hebrew University, Jerusalem 9190401, Israel.ORCID 0009-0008-4305-0282
Shira YochelisInstitute of Applied Physics, The Hebrew University, Jerusalem 9190401, Israel.ORCID 0000-0001-9180-4669
Daniel SharonInstitute of Chemistry, Hebrew University of Jerusalem, Jerusalem 91904, Israel.ORCID 0000-0002-3385-1536
Lech Tomasz BaczewskiInstitute of Physics, Polish Academy of Sciences, Warsaw 02668, Poland.
Ehud GazitThe Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 6997801, Israel.ORCID 0000-0001-5764-1720
Yossi PaltielInstitute of Applied Physics, The Hebrew University, Jerusalem 9190401, Israel.ORCID 0000-0002-8739-9952

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein aggregation into amyloid fibrils is central to numerous diseases, yet the role of electron spin interactions during nucleation and self-assembly remains unexplored. We investigated amyloid formation of A-β(1-42) polypeptide, implicated in Alzheimer's disease, and its smaller recognition motifs on ferromagnetic substrates. We observed a strong dependence of fibril formation dynamics on the substrate's magnetization orientation using electron and fluorescence microscopy. Specifically, one magnetization orientation yielded approximately twice as many and significantly longer (up to 20-fold) fibrils compared with the opposite orientation, a preference that flipped with the opposite monomer chirality. Furthermore, ATR-FTIR detected structural variations in the fibril structure, depending on the substrate magnetization. These findings suggest that transient spin polarization of the monomers during self-assembly, potentially driven by the Chiral-Induced Spin Selectivity (CISS) effect, plays a critical role in amyloid assembly dynamics. The consistency of these effects across different molecule length scales suggests a fundamental spin-based influence on biomolecular aggregation. This insight may have implications for therapeutic strategies, including the use of spin-polarized magnetic nanoparticles to selectively modulate amyloid formation in neurodegenerative diseases and the integration of spin-selective interfaces in dialysis systems to mitigate dialysis-related amyloidosis.

Indexed as

AmyloidAmyloid beta-PeptidesPeptide FragmentsHumansAmyloidAmyloid beta-Peptidesamyloid beta-protein (1-42)Peptide FragmentsamyloidsChiral-Induced Spin Selectivity (CISS)self-assemblyspin-controlled assembly dynamicsspin interactionsspin interfaces

Identifiers

PMID40717488
PMCPMC12356117

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.