Evidence map›Paper›PMID 38617345›Full record

ArticlebioRxiv : the preprint server for biology2024

Mag-Net: Rapid enrichment of membrane-bound particles enables high coverage quantitative analysis of the plasma proteome.

Christine C Wu, Kristine A Tsantilas, Jea Park, Deanna Plubell, Justin A Sanders, Previn Naicker, Ireshyn Govender, Sindisiwe Buthelezi, Stoyan Stoychev, Justin Jordaan and 9 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

19 authors.

Christine C WuDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Kristine A TsantilasDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Jea ParkDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Deanna PlubellDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Justin A SandersDepartment of Computer Science, University of Washington, Seattle, WA, USA.
Previn NaickerCSIR, Pretoria, South Africa.
Ireshyn GovenderReSyn Biosciences, Gauteng, South Africa.
Sindisiwe ButheleziCSIR, Pretoria, South Africa.
Stoyan StoychevReSyn Biosciences, Gauteng, South Africa.
Justin JordaanReSyn Biosciences, Gauteng, South Africa.
Gennifer MerrihewDepartment of Computer Science, University of Washington, Seattle, WA, USA.ORCID 0000-0003-4903-0318
Eric HuangDepartment of Computer Science, University of Washington, Seattle, WA, USA.
Edward D ParkerVision Core Lab, Department of Ophthalmology, University of Washington, Seattle, WA, USA.
Michael RiffleDepartment of Biochemistry, University of Washington, Seattle, WA, USA.
Andrew N HoofnagleDepartment of Lab Medicine and Pathology, University of Washington, Seattle, WA, USA.
William S NobleDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0001-7283-4715
Kathleen L PostonDepartment of Neurology & Neurological Sciences, Stanford University, Palo Alto CA, USA.ORCID 0000-0003-3424-7143
Thomas J MontineDepartment of Pathology, Stanford University, Palo Alto CA, USA.ORCID 0000-0002-1346-2728
Michael J MacCossDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID 0000-0003-1853-0256

Funding

Stanford Alzheimer's Disease Research CenterAdmin Supp: Developing iPSC models for AD and PDP30AG066515 · NIA · STANFORD UNIVERSITY · PI Lisa Goldman Rosas · 2020 to 2026
$29.0M
University of Washington Nathan Shock Center of Excellence in the Basic Biology of AgingP30AG013280 · NIA · UNIVERSITY OF WASHINGTON · PI Maitreya J Dunham · 1995 to 2026
$27.1M
Project 4: Novel reagent development to enable molecular characterizationU19AG065156 · NIA · UNIVERSITY OF WASHINGTON · PI MACCOSS, MICHAEL · 2020 to 2024
$15.9M
Biological Mechanisms of Healthy Aging Training GrantT32AG066574 · NIA · UNIVERSITY OF WASHINGTON · PI David J. Marcinek, Jessica E Young · 2020 to 2026
$5.3M
The impact of early Tau pathology on cognitive progression and neuropsychiatric symptoms in Parkinson's diseaseR01NS115114 · NINDS · STANFORD UNIVERSITY · PI ANDREASSON, KATRIN I., POSTON, KATHLEEN LOMBARD · 2019 to 2023
$4.2M
Quantifying proteins in plasma do democratize personalized medicine for patients with type 1 diabetesU01DK137097 · NIDDK · UNIVERSITY OF WASHINGTON · PI ANDREW N HOOFNAGLE, Michael MacCoss · 2023 to 2026
$3.4M
Quantifying proteins in plasma to democratize personalized medicine for patients with type 1 diabetesU01DK121289 · NIDDK · UNIVERSITY OF WASHINGTON · PI HOOFNAGLE, ANDREW N · 2019 to 2021
$1.9M
Proteolytic activity profiling of Alzheimer's dementiaF31AG069420 · NIA · UNIVERSITY OF WASHINGTON · PI PLUBELL, DEANNA LISA · 2020 to 2021
$81k
NIA NIH HHS F31 AG069420NIA NIH HHS P30 AG013280NIA NIH HHS P30 AG066515NIA NIH HHS T32 AG066574NIA NIH HHS U19 AG065156NIDDK NIH HHS U01 DK121289NIDDK NIH HHS U01 DK137097NINDS NIH HHS R01 NS115114
6 · The paper itself

Abstract

Membrane-bound particles in plasma are composed of exosomes, microvesicles, and apoptotic bodies and represent ~1-2% of the total protein composition. Proteomic interrogation of this subset of plasma proteins augments the representation of tissue-specific proteins, representing a "liquid biopsy," while enabling the detection of proteins that would otherwise be beyond the dynamic range of liquid chromatography-tandem mass spectrometry of unfractionated plasma. We have developed an enrichment strategy (Mag-Net) using hyper-porous strong-anion exchange magnetic microparticles to sieve membrane-bound particles from plasma. The Mag-Net method is robust, reproducible, inexpensive, and requires <100 μL plasma input. Coupled to a quantitative data-independent mass spectrometry analytical strategy, we demonstrate that we can collect results for >37,000 peptides from >4,000 plasma proteins with high precision. Using this analytical pipeline on a small cohort of patients with neurodegenerative disease and healthy age-matched controls, we discovered 204 proteins that differentiate (q-value < 0.05) patients with Alzheimer's disease dementia (ADD) from those without ADD. Our method also discovered 310 proteins that were different between Parkinson's disease and those with either ADD or healthy cognitively normal individuals. Using machine learning we were able to distinguish between ADD and not ADD with a mean ROC AUC = 0.98 ± 0.06.

Identifiers

PMID38617345
PMCPMC11014469

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.