Evidence map›Paper›PMID 31308243›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Fluorescence spectral shape analysis for nucleotide identification.

Yun Huang, Zhiliang Li, April L Risinger, Benjamin T Enslow, Charles J Zeman, Jiang Gong, Yajing Yang, Kirk S Schanze

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
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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

8 authors.

Yun HuangDepartment of Chemistry, University of Texas at San Antonio, San Antonio, TX 78249.ORCID 0000-0001-5438-5522
Zhiliang LiDepartment of Chemistry, University of Texas at San Antonio, San Antonio, TX 78249.
April L RisingerDepartment of Pharmacology, University of Texas Health Science Center, San Antonio, TX 78229; risingera@uthscsa.edu Kirk.Schanze@utsa.edu.ORCID 0000-0002-4363-3268
Benjamin T EnslowLong School of Medicine, University of Texas Health Science Center, San Antonio, TX 78229.
Charles J ZemanDepartment of Chemistry, University of Texas at San Antonio, San Antonio, TX 78249.ORCID 0000-0001-5275-0469
Jiang GongKey Laboratory for Material Chemistry of Energy Conversion and Storage, Ministry of Education, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, 430074 Wuhan, People's Republic of China.
Yajing YangDepartment of Chemistry, University of Texas at San Antonio, San Antonio, TX 78249.
Kirk S SchanzeDepartment of Chemistry, University of Texas at San Antonio, San Antonio, TX 78249; risingera@uthscsa.edu Kirk.Schanze@utsa.edu.ORCID 0000-0003-3342-4080

Funding

San Antonio Biomedical Education and ResearchK12GM111726 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LECHLEITER, JAMES D, OYAJOBI, BABATUNDE OLUKAYODE · 2015 to 2024
$7.6M
NIGMS NIH HHS K12 GM111726
6 · The paper itself

Abstract

We report a conjugated polyelectrolyte fluorescence-based biosensor P-C-3 and a general methodology to evaluate spectral shape recognition to identify biomolecules using artificial intelligence. By using well-defined analytes, we demonstrate that the fluorescence spectral shape of P-C-3 is sensitive to minor structural changes and exhibits distinct signature patterns for different analytes. A method was also developed to select useful features to reduce computational complexity and prevent overfitting of the data. It was found that the normalized intensity of 3 to 5 selected wavelengths was sufficient for the fluorescence biosensor to classify 13 distinct nucleotides and distinguish as little as single base substitutions at distinct positions in the primary sequence of oligonucleotides rapidly with nearly 100% classification accuracy. Photophysical studies led to a model to explain the mechanism of these fluorescence spectral shape changes, which provides theoretical support for applying this method in complicated biological systems. Using the feature selection algorithm to measure the relative intensity of a few selected wavelengths significantly reduces measurement time, demonstrating the potential for fluorescence spectrum shape analysis in high-throughput and high-content screening.

Indexed as

Discriminant AnalysisLightNucleotidesSpectrometry, FluorescenceTime FactorsNucleotidesbiosensorfluorescencemachine learningnucleic acidsphosphate sensing

Identifiers

PMID31308243
PMCPMC6681718

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.