Evidence map›Paper›PMID 30909588›Full record

ArticleSensors (Basel, Switzerland)2019

LSPR Biosensing Approach for the Detection of Microtubule Nucleation.

Keisuke Hasegawa, Otabek Nazarov, Evan Porter

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2019. 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

3 authors.

Keisuke HasegawaDepartment of Physics, Grinnell College, 1116 Eighth Avenue, Grinnell, IA 50112, USA. hasegawa@grinnell.edu.
Otabek NazarovDepartment of Physics, Grinnell College, 1116 Eighth Avenue, Grinnell, IA 50112, USA. nazarovo@grinnell.edu.
Evan PorterDepartment of Physics, Grinnell College, 1116 Eighth Avenue, Grinnell, IA 50112, USA. porterev17@grinnell.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microtubules are dynamic protein filaments that are involved in a number of cellular processes. Here, we report the development of a novel localized surface plasmon resonance (LSPR) biosensing approach for investigating one aspect of microtubule dynamics that is not well understood, namely, nucleation. Using a modified Mie theory with radially variable refractive index, we construct a theoretical model to describe the optical response of gold nanoparticles when microtubules form around them. The model predicts that the extinction maximum wavelength is sensitive to a change in the local refractive index induced by microtubule nucleation within a few tens of nanometers from the nanoparticle surface, but insensitive to a change in the refractive index outside this region caused by microtubule elongation. As a proof of concept to demonstrate that LSPR can be used for detecting microtubule nucleation experimentally, we induce spontaneous microtubule formation around gold nanoparticles by immobilizing tubulin subunits on the nanoparticles. We find that, consistent with the theoretical model, there is a redshift in the extinction maximum wavelength upon the formation of short microtubules around the nanoparticles, but no significant change in maximum wavelength when the microtubules are elongated. We also perform kinetic experiments and demonstrate that the maximum wavelength is sensitive to the microtubule nuclei assembly even when microtubules are too small to be detected from an optical density measurement.

Indexed as

Surface Plasmon ResonanceAnimalsBiosensing TechniquesGoldKineticsMetal NanoparticlesMicroscopy, FluorescenceMicrotubulesModels, TheoreticalPolyethylene GlycolsSwineTubulinGoldPolyethylene GlycolsTubulingold nanoparticleslocalized surface plasmon resonancemicrotubule nucleationoptical biosensors

Identifiers

PMID30909588
PMCPMC6471214

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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.