Evidence map›Paper›PMID 40207094›Full record

ArticleRNA nanomed2024

Applications of Surface Plasmon Resonance for Advanced Studies Involving Nucleic Acids.

Katelynn Pranger, Kenya Rosas, Dmitriy Khon, Emil F Khisamutdinov

Abstract read
In one paragraph

Article in RNA nanomed, 2024. 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. 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

4 authors.

Katelynn PrangerDepartment of Chemistry, Ball State University, Muncie, IN 47306, USA.
Kenya RosasDepartment of Chemistry and Biochemistry, St. Mary's University, San Antonio, TX 78228, USA.
Dmitriy KhonDepartment of Chemistry and Biochemistry, St. Mary's University, San Antonio, TX 78228, USA.
Emil F KhisamutdinovDepartment of Chemistry, Ball State University, Muncie, IN 47306, USA.

Funding

Nucleic Acid Nanoparticle-based Monoclonal Antibody MimicsR15EB031388 · NIBIB · BALL STATE UNIVERSITY · PI KHISAMUTDINOV, EMIL · 2021 to 2025
$1.0M
NIBIB NIH HHS R15 EB031388
6 · The paper itself

Abstract

Surface plasmon resonance (SPR) is increasingly recognized as one of the most widely used techniques for studying nucleic acid interactions. The main advantage of SPR is its ability to measure the binding affinities and association/dissociation kinetics of complexes in real-time, in a label-free environment, and using relatively small quantities of materials. The method is based on the immobilization of one of the binding partners, ligand, on a dedicated sensor surface. Immobilization is followed by the injection of the other partner, analyte, over the surface containing the ligand. The binding is monitored by subsequent changes in the refractive index of the medium close to the sensor surface upon injection of the analyte. In the field of Nucleic Acid, SPR has been intensively used in the study of various artificial and naturally occurring RNA/DNA molecules interaction with large molecular weight mass proteins and small organic molecules because of its ability to detect highly dynamic complexes that are difficult to investigate using other techniques. This mini review aims to provide a short guideline for setting up SPR experiments to identify nucleic acid complexes and assess their binding affinity or kinetics. It covers protocols for (i) nucleic acid immobilization methods, including biotin-streptavidin, metal ion-based affinity, and amine coupling, (ii) analyte-binding analysis, (iii) affinity and kinetic measurements, and (iv) data interpretation. Determining the affinity and kinetics of nucleic acid interactions through SPR is essential for gaining insights into molecular-level binding mechanisms, thus supporting advancements in nucleic acid nanotechnology. The review also highlights the various sections of SPR applications in nucleic acid research, including nucleic acid-probe immobilization, interactions with biomolecules, aptamer studies, and small molecule binding, concluding with perspectives on future developments in the field.

Indexed as

BioconjugationBiophysicsDissociation ConstantNucleic Acid Nanoparticles

Identifiers

PMID40207094
PMCPMC11981602

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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.