Evidence map›Paper›PMID 31533330›Full record

ArticleBiosensors2019

Characterization of Binding of Magnetic Nanoparticles to Rolling Circle Amplification Products by Turn-On Magnetic Assay.

Sobhan Sepehri, Björn Agnarsson, Teresa Zardán Gómez de la Torre, Justin F Schneiderman, Jakob Blomgren, Aldo Jesorka, Christer Johansson, Mats Nilsson, Jan Albert, Maria Strømme and 2 more

Abstract read
In one paragraph

Article in Biosensors, 2019. 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

12 authors.

Sobhan SepehriDepartment of Microtechnology and Nanoscience-MC2, Chalmers University of Technology, SE-412 96 Göteborg, Sweden. sobhan.sepehri@chalmers.se.ORCID 0000-0002-2145-1340
Björn AgnarssonDepartment of Physics, Chalmers University of Technology, SE-412 96 Göteborg, Sweden. bjorn.agnarsson@chalmers.se.
Teresa Zardán Gómez de la TorreDepartment of Engineering Sciences, Uppsala University, The Ångström Laboratory, Box 534, SE-751 21 Uppsala, Sweden. Teresa.Zardan@angstrom.uu.se.
Justin F SchneidermanDepartment of Microtechnology and Nanoscience-MC2, Chalmers University of Technology, SE-412 96 Göteborg, Sweden. justin.schneiderman@neuro.gu.se.
Jakob BlomgrenRISE-Research Institutes of Sweden, SE-411 33 Göteborg, Sweden. jakob.blomgren@ri.se.ORCID 0000-0002-6148-3574
Aldo JesorkaDepartment of Chemistry and Chemical Engineering, Chalmers University of Technology, SE-412 96 Göteborg, Sweden. aldo@chalmers.se.
Christer JohanssonRISE-Research Institutes of Sweden, SE-411 33 Göteborg, Sweden. christer.johansson@ri.se.
Mats NilssonScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Box 1031, SE-171 21 Solna, Sweden. mats.nilsson@scilifelab.se.
Jan AlbertDepartment of Clinical Microbiology, Karolinska University Hospital, SE-171 76 Stockholm, Sweden. jan.albert@ki.se.
Maria StrømmeDepartment of Engineering Sciences, Uppsala University, The Ångström Laboratory, Box 534, SE-751 21 Uppsala, Sweden. maria.stromme@angstrom.uu.se.
Dag WinklerDepartment of Microtechnology and Nanoscience-MC2, Chalmers University of Technology, SE-412 96 Göteborg, Sweden. dag.winkler@chalmers.se.
Alexei KalaboukhovDepartment of Microtechnology and Nanoscience-MC2, Chalmers University of Technology, SE-412 96 Göteborg, Sweden. alexei.kalaboukhov@chalmers.se.

Funding

Stiftelsen för Strategisk Forskning SBE13-0125Vetenskapsrådet 2015-03640
6 · The paper itself

Abstract

The specific binding of oligonucleotide-tagged 100 nm magnetic nanoparticles (MNPs) to rolling circle products (RCPs) is investigated using our newly developed differential homogenous magnetic assay (DHMA). The DHMA measures ac magnetic susceptibility from a test and a control samples simultaneously and eliminates magnetic background signal. Therefore, the DHMA can reveal details of binding kinetics of magnetic nanoparticles at very low concentrations of RCPs. From the analysis of the imaginary part of the DHMA signal, we find that smaller MNPs in the particle ensemble bind first to the RCPs. When the RCP concentration increases, we observe the formation of agglomerates, which leads to lower number of MNPs per RCP at higher concentrations of RCPs. The results thus indicate that a full frequency range of ac susceptibility observation is necessary to detect low concentrations of target RCPs and a long amplification time is not required as it does not significantly increase the number of MNPs per RCP. The findings are critical for understanding the underlying microscopic binding process for improving the assay performance. They furthermore suggest DHMA is a powerful technique for dynamically characterizing the binding interactions between MNPs and biomolecules in fluid volumes.

Indexed as

Biosensing TechniquesMagnetite NanoparticlesMagnetite Nanoparticlesbinding kineticsbioassaydifferential homogenous magnetic assayimmobilizationmagnetic nanoparticlerolling circle amplification product

Identifiers

PMID31533330
PMCPMC6784358

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.