Evidence map›Paper›PMID 41116299›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Reversible Sandwich-Based Particle Nanoswitch for Continuous Protein Monitoring at Picomolar Concentrations with Automated Calibration.

Claire M S Michielsen, Junhong Yan, Max H Bergkamp, Yu-Ting Lin, Stijn R R Haenen, Rafiq M Lubken, Alexander Gräwe, Anna Swietlikowska, Arthur M de Jong, Menno W J Prins

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

10 authors.

Claire M S MichielsenDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, 5612 AZ, The Netherlands.ORCID 0000-0002-8580-8695
Junhong YanHelia Biomonitoring BV, Eindhoven, 5612 AR, The Netherlands.ORCID 0000-0002-2332-2315
Max H BergkampHelia Biomonitoring BV, Eindhoven, 5612 AR, The Netherlands.ORCID 0000-0001-8904-4322
Yu-Ting LinHelia Biomonitoring BV, Eindhoven, 5612 AR, The Netherlands.ORCID 0000-0003-3235-9491
Stijn R R HaenenHelia Biomonitoring BV, Eindhoven, 5612 AR, The Netherlands.ORCID 0009-0006-6194-0102
Rafiq M LubkenHelia Biomonitoring BV, Eindhoven, 5612 AR, The Netherlands.ORCID 0000-0001-7554-1141
Alexander GräweDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, 5612 AZ, The Netherlands.ORCID 0000-0003-2892-278X
Anna SwietlikowskaDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, 5612 AZ, The Netherlands.ORCID 0009-0008-7289-7642
Arthur M de JongInstitute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, 5612 AZ, The Netherlands.ORCID 0000-0001-6019-7333
Menno W J PrinsDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, 5612 AZ, The Netherlands.ORCID 0000-0002-9788-7298

Funding

The Netherlands National Growth Fund Programme NXTGEN HighTechThe Netherlands Topsector Agri&Food, HTSM, and Chemistry LWV20.117
6 · The paper itself

Abstract

Continuous monitoring of specific proteins is essential for understanding the dynamics of biological systems and for enabling real-time measurement-and-control strategies in bioprocesses. Ideally, sensors for continuous monitoring should be intrinsically reversible and able to perform accurate measurements over long time spans. Here, we present a particle nanoswitch sensor containing two different antibody fragments that bind reversibly to a protein of interest and thus form transient sandwich complexes. The antibody fragments are incorporated into the sensor using site-specific conjugation strategies to achieve optimal antibody orientation. Short-lived sandwich complexes are detected with single-molecule resolution, by tracking the motion of tethered particles. The sensing concept is demonstrated for lactoferrin, an iron-binding and immune-modulating protein. We show continuous measurements of picomolar concentrations, with a delay time of less than 12 min, over a monitoring period of more than 12 h. Automated calibration strategies are described that result in a mean absolute relative difference below 10% compared to reference measurements. These results demonstrate how rapid continuous protein sensing at picomolar concentrations can be achieved using reversible sandwich-based particle nanoswitches, enabling long-term monitoring of dynamic bioprocesses.

Indexed as

Biosensing TechniquesLactoferrinProteinsCalibrationLactoferrinProteinsAntibody‐based biosensingContinuous biosensingParticle nanoswitchPicomolar concentrationsProtein monitoring

Identifiers

PMID41116299
PMCPMC12707359

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.