Evidence map›Paper›PMID 42666124›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Machine-Learning-Assisted Impedance Component Analysis Enables Standardizable Surface Protein Analysis of Extracellular Vesicles Using Engineered Nanovesicles.

Jaeyoon Song, Neethu Ramakrishnan, Sehyeon Kim, Huiseop Lee, Youngeun Kwon, Jinsik Kim

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Jaeyoon SongDepartment of Biomedical Engineering, College of Life Science and Biotechnology, Dongguk University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0001-5663-238X
Neethu RamakrishnanDepartment of Biomedical Engineering, College of Life Science and Biotechnology, Dongguk University, Seoul, Republic of Korea.
Sehyeon KimDepartment of Biomedical Engineering, College of Life Science and Biotechnology, Dongguk University, Seoul, Republic of Korea.
Huiseop LeeDepartment of Biomedical Engineering, College of Life Science and Biotechnology, Dongguk University, Seoul, Republic of Korea.
Youngeun KwonDepartment of Biomedical Engineering, College of Life Science and Biotechnology, Dongguk University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-6568-6010
Jinsik KimDepartment of Biomedical Engineering, College of Life Science and Biotechnology, Dongguk University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0002-9121-7031

Funding

Commercialization Promotion Agency for R&D Outcomes RS-2025-17632971National Research Foundation of Korea 2023R1A2C2007147National Research Foundation of Korea RS-2024-00416117
6 · The paper itself

Abstract

Characterizing surface protein heterogeneity on extracellular vesicles remains challenging but essential for understanding their biological functions and clinical applications. Here, this study introduces an integrated platform that combines engineered cell-derived nanovesicles, used as model standards with controlled surface protein states, and machine learning-optimized impedance spectroscopy. Cell-derived nanovesicles with defined surface protein densities are generated by extruding HeLa cells expressing 1, 3, or 9 copies of amyloid-β 42, establishing a series of reference vesicles with precisely controlled oligomeric configurations. Through systematic evaluation of impedance features across frequencies from 10 Hz to 1 MHz, machine learning identifies reactance changes at 1 kHz as optimal for distinguishing oligomeric states on the vesicle membrane. Equivalent-circuit modeling reveals that membrane capacitance correlates with protein oligomerization, and structural predictions explain the mechanistic basis. The platform also enables label-free, time-resolved analysis of Aβ oligomer formation directly on vesicular membranes, providing insights into aggregation dynamics. This platform establishes standardizable reference materials using engineered nanovesicles and a quantitative framework for extracellular vesicle surface protein analysis, offering a broadly applicable method for studying membrane-associated protein dynamics relevant to neurodegenerative diseases and advancing extracellular vesicle-based diagnostics.

Indexed as

amyloid betaengineered nanovesiclesextracellular vesiclesimpedance spectroscopymachine learning

Identifiers

PMID42666124
PMCPMC13525417

What Socratic holds

Textmetadata
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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 Socratic graph.