OSCR

Distinct Filament Conformation for Receptor-Bound Amyloid-β from Alzheimer's Disease Brain.

Overview

Authors: Mikhail A Kostylev1, Carmen Butan1, Graham P Roseman1, Yangyi Liu1, Tanina Arab1, Ruibing Wu1, Pallavi Gopal2, Stephen M Strittmatter1,3
  1. Departments of Neuroscience, Yale School of Medicine, New Haven, CT USA
  2. Department of Pathology, Yale School of Medicine, New Haven, CT USA
  3. Department of Neurology, Yale School of Medicine, New Haven, CT USA
Institutions: Yale University (United States)
Journal: Nature communications, volume 17, issue 1, article 8953
Dates: received 21 November 2024; accepted 9 July 2026; published online 22 July 2026
Type: Research article · Language: English
License: CC BY-NC-ND
Identifiers: DOI 10.1038/s41467-026-75895-9 · PMID 42637746 · PMCID PMC13503723 · OpenAlex W4415126098
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: histology / microscopy (modality), human (organism), other condition (population), Alzheimer's / dementia (population), cellular / molecular (subfield)
Methods: fMRI & imaging
Keywords: Alzheimer's disease, Cryoelectron microscopy
MeSH: Alzheimer Disease*, Amyloid beta-Peptides*, Brain*, Animals, Cryoelectron Microscopy, Humans, Neurons, Plaque, Amyloid, Prions, Protein Binding, Protein Conformation, Synapses (* major topic)
Topic: Alzheimer's disease research and treatments (Physiology, Medicine), according to OpenAlex
Funding: U.S. Department of Health & Human Services | National Institutes of Health (P30AG066508, T32NS105583, R01AG034924); NIA NIH HHS (R01 AG034924, P30 AG066508); U.S. Department of Health & Human Services | National Institutes of Health (NIH) (T32NS105583, P30AG066508, R01AG034924); NINDS NIH HHS (T32 NS105583)
Citations: not cited yet (Europe PMC); 72 references in the paper

Abstract

The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.

Code

The paper links to its data, not to its authors' code: see the Data section.

The paper's code and data availability statement is in the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Code and data availability statement

The paper has a code and data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:

Read it in the paper: doi.org/10.1038/s41467-026-75895-9.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 2 keywords, 12 MeSH terms, 4 funders, 71 references.

Cite

This paper

Kostylev, M. A., Butan, C., Roseman, G. P., Liu, Y., Arab, T., Wu, R., Gopal, P., & Strittmatter, S. M. (2026). Distinct Filament Conformation for Receptor-Bound Amyloid-β from Alzheimer's Disease Brain. Nature communications, 17(1), 8953. https://doi.org/10.1038/s41467-026-75895-9

BibTeX

@article{kostylev2026distinct,
author = {Kostylev, Mikhail A and Butan, Carmen and Roseman, Graham P and Liu, Yangyi and Arab, Tanina and Wu, Ruibing and Gopal, Pallavi and Strittmatter, Stephen M},
title = {{Distinct Filament Conformation for Receptor-Bound Amyloid-β from Alzheimer's Disease Brain}},
journal = {Nature communications},
year = {2026},
month = jul,
volume = {17},
number = {1},
pages = {8953},
publisher = {Nature Publishing Group},
issn = {2041-1723},
doi = {10.1038/s41467-026-75895-9},
url = {https://doi.org/10.1038/s41467-026-75895-9},
pmid = {42637746},
pmcid = {PMC13503723}
}

RIS

TY - JOUR
AU - Kostylev, Mikhail A
AU - Butan, Carmen
AU - Roseman, Graham P
AU - Liu, Yangyi
AU - Arab, Tanina
AU - Wu, Ruibing
AU - Gopal, Pallavi
AU - Strittmatter, Stephen M
TI - Distinct Filament Conformation for Receptor-Bound Amyloid-β from Alzheimer's Disease Brain
T2 - Nature communications
J2 - Nat Commun
PY - 2026
DA - 2026/07/22
VL - 17
IS - 1
SP - 8953
SN - 2041-1723
PB - Nature Publishing Group
DO - 10.1038/s41467-026-75895-9
UR - https://doi.org/10.1038/s41467-026-75895-9
LA - en
ER -

CSL-JSON

{
"id": "10.1038/s41467-026-75895-9",
"type": "article-journal",
"title": "Distinct Filament Conformation for Receptor-Bound Amyloid-β from Alzheimer's Disease Brain",
"container-title": "Nature communications",
"author": [
{
"family": "Kostylev",
"given": "Mikhail A"
},
{
"family": "Butan",
"given": "Carmen"
},
{
"family": "Roseman",
"given": "Graham P"
},
{
"family": "Liu",
"given": "Yangyi"
},
{
"family": "Arab",
"given": "Tanina"
},
{
"family": "Wu",
"given": "Ruibing"
},
{
"family": "Gopal",
"given": "Pallavi"
},
{
"family": "Strittmatter",
"given": "Stephen M"
}
],
"container-title-short": "Nat Commun",
"volume": "17",
"issue": "1",
"page": "8953",
"DOI": "10.1038/s41467-026-75895-9",
"PMID": "42637746",
"PMCID": "PMC13503723",
"ISSN": "2041-1723",
"publisher": "Nature Publishing Group",
"URL": "https://doi.org/10.1038/s41467-026-75895-9",
"language": "en",
"issued": {
"date-parts": [
[
2026,
7,
22
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1016/j.celrep.2026.117599
Immunotherapy with B28, an antibody to Aβ oligomers, potently decreases amyloid plaques, microgliosis, and memory decline in APP knock-in mice.
Journal: Cell reports
In common: Alzheimer's / dementia, cellular / molecular, 5 references
[2] doi:10.7554/elife.104778 [code]
Twelve phosphomimetic mutations induce the assembly of recombinant full-length human tau into paired helical filaments.
Journal: eLife
In common: histology / microscopy, Alzheimer's / dementia, cellular / molecular, 4 references
[3] doi:10.1038/s41467-026-76831-7
Structural origins of species-specific differences in TRPV2 activation.
Journal: Nature communications
In common: histology / microscopy, cellular / molecular, 4 references
[4] doi:10.1038/s41467-026-75564-x
Cooperative mechanism of neurotransmitter recognition and transport by the human vesicular polyamine transporter.
Journal: Nature communications
In common: histology / microscopy, cellular / molecular, 4 references
[5] doi:10.1038/s41467-026-76368-9
Integrative structural analysis of human endosomal NHE6 reveals a lipid-associated gate and disordered C-terminus.
Journal: Nature communications
In common: histology / microscopy, cellular / molecular, 4 references
[6] doi:10.1016/j.stemcr.2026.102924
PrP<sup>C</sup>-facilitated cell signaling activates phospholipase Cɣ1 and triggers an Arc/Arg3.1 response in mouse and iPSC-derived human neurons.
Journal: Stem cell reports
In common: Alzheimer's / dementia, other condition, cellular / molecular, 3 references
[7] doi:10.3389/fimmu.2026.1937738
Multi-regional transcriptomic analysis reveals early nociceptive and neuroinflammatory alterations in APP/PS1 mice.
Journal: Frontiers in immunology
In common: Alzheimer's / dementia, cellular / molecular, 3 references
[8] doi:10.1186/s40478-026-02324-9
Characterization of a distinct form of vimentin in the neurodegenerative brain.
Journal: Acta neuropathologica communications
In common: Alzheimer's / dementia, cellular / molecular, 3 references
[9] doi:10.3390/ijms27083430
Metatranscriptomic Reanalysis of Alzheimer's Brains Identifies Low-Biomass Microbial Signals Including Enrichment of <i>Acinetobacter radioresistens</i>.
Journal: International journal of molecular sciences
In common: Alzheimer's / dementia, 4 references
[10] doi:10.1038/s41594-026-01787-7 [code]
Microtubules in the axon are GDP bound but adopt a stable GTP-like expanded state.
Journal: Nature structural & molecular biology
In common: histology / microscopy, cellular / molecular, 3 references

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.