Evidence map›Paper›PMID 32614597›Full record

ArticleJournal of proteome research2020

Magnetic Synthetic Receptors for Selective Clean-Up in Protein Biomarker Quantification.

Nicholas McKitterick, Frida Braathen, Magdalena A Switnicka-Plak, Peter A G Cormack, Léon Reubsaet, Trine Grønhaug Halvorsen

Open access · hybridAbstract read
In one paragraph

Article in Journal of proteome research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 25% of its field
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

2 citing papers in PubMed, 14 citations in OpenAlex.

  1. Magnetic Nanomaterials for Sample Preparation of Disease-related Biomarkers.Combinatorial chemistry & high throughput screening · 2025
    Review
  2. Review
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 at 2 institutions in 2 countries.

Nicholas McKitterickSection for Pharmaceutical Chemistry, Department of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.
Frida BraathenSection for Pharmaceutical Chemistry, Department of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.
Magdalena A Switnicka-PlakWestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, Thomas Graham Building, 295 Cathedral Street, Glasgow G1 1XL, Scotland, U.K.
Peter A G CormackWestCHEM, Department of Pure and Applied Chemistry, University of Strathclyde, Thomas Graham Building, 295 Cathedral Street, Glasgow G1 1XL, Scotland, U.K.
Léon ReubsaetSection for Pharmaceutical Chemistry, Department of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.ORCID 0000-0001-5165-2701
Trine Grønhaug HalvorsenSection for Pharmaceutical Chemistry, Department of Pharmacy, University of Oslo, PO Box 1068 Blindern, 0316 Oslo, Norway.ORCID 0000-0002-2545-3474
University of Oslo · NOUniversity of Strathclyde · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biomarker analysis by mass spectrometry (MS) can allow for the rapid quantification of low abundant biomarkers. However, the complexity of human serum is a limiting factor in MS-based bioanalysis; therefore, novel biomarker enrichment strategies are of interest, particularly if the enrichment strategies are of low cost and are easy to use. One such strategy involves the use of molecularly imprinted polymers (MIPs) as synthetic receptors for biomarker enrichment. In the present study, a magnetic solid-phase extraction (mSPE) platform, based on magnetic MIP (mMIP) sorbents, is disclosed, for use in the MS-based quantification of proteins by the bottom-up approach. Progastrin releasing peptide (ProGRP), a low abundant and clinically sensitive biomarker for small cell lung cancer (SCLC), was used to exemplify the mSPE platform. Four different mMIPs were synthesized, and an mSPE method was developed and optimized for the extraction of low concentrations of tryptic peptides from human serum. The mSPE method enabled the selective extraction of the ProGRP signature peptide, the nonapeptide NLLGLIEAK, prior to quantification of the target via LC-MS/MS. Overall, the mSPE method demonstrated its potential as a low cost, rapid, and straightforward sample preparation method, with demonstrably strong binding, acceptable recoveries, and good compatibility with MS. mMIPs are a potential low-cost alternative to current clinical methods for biomarker analysis.

Indexed as

Lung NeoplasmsReceptors, ArtificialBiomarkersChromatography, LiquidHumansMagnetic PhenomenaSolid Phase ExtractionTandem Mass SpectrometryBiomarkersReceptors, Artificialbottom-up protein analysisLC-MS/MSlow-abundant biomarkersmagnetic capturemolecularly imprinted polymers

Identifiers

PMID32614597
PMCPMC7467826
OpenAlexW3039627173

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.