Evidence map›Paper›PMID 31811474›Full record

ReviewAnnals of biomedical engineering2020

The Convergence of Cell-Based Surface Plasmon Resonance and Biomaterials: The Future of Quantifying Bio-molecular Interactions-A Review.

Spencer B Mamer, Phillip Page, Mary Murphy, Jiaojiao Wang, Pierrick Gallerne, Ali Ansari, P I Imoukhuede

Abstract readReview
In one paragraph

Review in Annals of biomedical engineering, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Target Engagement Assays in Early Drug Discovery.Journal of medicinal chemistry · 2025
    Review
  8. Review
  9. Article
  10. Label-free methods for opticalPhysical chemistry chemical physics : PCCP · 2021
    Review
  11. 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

7 authors.

Spencer B MamerDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.ORCID http://orcid.org/0000-0002-5613-3596
Phillip PageReichert, Inc., Depew, NY, USA.
Mary MurphyReichert, Inc., Depew, NY, USA.
Jiaojiao WangDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Pierrick GallerneDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Ali AnsariDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
P I ImoukhuedeDepartment of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO, USA. imoukhuede@wustl.edu.

Funding

Quantitative and computational characterization of oxytocin receptor signaling: Administrative supplementR01HD096737 · NICHD · WASHINGTON UNIVERSITY · PI ENGLAND, SARAH K., IMOUKHUEDE, PRINCESS IZEVBUA · 2019 to 2023
$2.8M
National Science Foundation 1743333NICHD NIH HHS R01 HD096737
6 · The paper itself

Abstract

Cell biology is driven by complex networks of biomolecular interactions. Characterizing the kinetic and thermodynamic properties of these interactions is crucial to understanding their role in different physiological processes. Surface plasmon resonance (SPR)-based approaches have become a key tool in quantifying biomolecular interactions, however conventional approaches require isolating the interacting components from the cellular system. Cell-based SPR approaches have recently emerged, promising to enable precise measurements of biomolecular interactions within their normal biological context. Two major approaches have been developed, offering their own advantages and limitations. These approaches currently lack a systematic exploration of 'best practices' like those existing for traditional SPR experiments. Toward this end, we describe the two major approaches, and identify the experimental parameters that require exploration, and discuss the experimental considerations constraining the optimization of each. In particular, we discuss the requirements of future biomaterial development needed to advance the cell-based SPR technique.

Indexed as

Biocompatible MaterialsBiosensing TechniquesSurface Plasmon ResonanceCell AdhesionCells, ImmobilizedHumansKineticsSystems BiologyBiocompatible MaterialsBiomolecular interactionsCell-based SPRSurface plasmon resonance (SPR)Systems biology

Identifiers

PMID31811474
PMCPMC8637426

What OpenQuestion holds

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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 OpenQuestion graph.