Evidence map›Paper›PMID 31936438›Full record

ArticleNanomaterials (Basel, Switzerland)2020

Hierarchical Cluster Analysis of Medical Chemicals Detected by a Bacteriophage-Based Colorimetric Sensor Array.

Chuntae Kim, Hansong Lee, Vasanthan Devaraj, Won-Geun Kim, Yujin Lee, Yeji Kim, Na-Na Jeong, Eun Jung Choi, Sang Hong Baek, Dong-Wook Han and 2 more

Abstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Application of Bacteriophages in Nanotechnology.Nanomaterials (Basel, Switzerland) · 2020
    Review
  12. Article
  13. Article
  14. Virus-Based Nanomaterials and Nanostructures.Nanomaterials (Basel, Switzerland) · 2020
    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

12 authors.

Chuntae KimDepartment of Nanofusion Technology, Pusan National University, Busan 46241, Korea.
Hansong LeeInterdisciplinary Program of Genomic Data Science, Pusan National University, Busan 46241, Korea.
Vasanthan DevarajResearch Center for Energy Convergence and Technology, Pusan National University, Busan 46241, Korea.ORCID 0000-0002-2181-800X
Won-Geun KimDepartment of Nanofusion Technology, Pusan National University, Busan 46241, Korea.
Yujin LeeDepartment of Nanofusion Technology, Pusan National University, Busan 46241, Korea.
Yeji KimDepartment of Nanofusion Technology, Pusan National University, Busan 46241, Korea.
Na-Na JeongBK21PLUS Program in Embodiment: Health-Society Interaction, Department of Public Health Sciences, Graduate School, Korea University, Seoul 02841, Korea.
Eun Jung ChoiResearch Center for Energy Convergence and Technology, Pusan National University, Busan 46241, Korea.
Sang Hong BaekLaboratory of Cardiovascular Disease, Division of Cardiology, School of Medicine, The Catholic University of Korea, Seoul 06591, Korea.ORCID 0000-0002-7065-3432
Dong-Wook HanDepartment of Cogno-Mechatronics Engineering, College of Nanoscience & Nanotechnology, Pusan National University, Busan 46241, Korea.ORCID 0000-0001-8314-1981
Hokeun SunInterdisciplinary Program of Genomic Data Science, Pusan National University, Busan 46241, Korea.
Jin-Woo OhDepartment of Nanofusion Technology, Pusan National University, Busan 46241, Korea.ORCID 0000-0002-0065-5088

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

M13 bacteriophage-based colorimetric sensors, especially multi-array sensors, have been successfully demonstrated to be a powerful platform for detecting extremely small amounts of target molecules. Colorimetric sensors can be fabricated easily using self-assembly of genetically engineered M13 bacteriophage which incorporates peptide libraries on its surface. However, the ability to discriminate many types of target molecules is still required. In this work, we introduce a statistical method to efficiently analyze a huge amount of numerical results in order to classify various types of target molecules. To enhance the selectivity of M13 bacteriophage-based colorimetric sensors, a multi-array sensor system can be an appropriate platform. On this basis, a pattern-recognizing multi-array biosensor platform was fabricated by integrating three types of sensors in which genetically engineered M13 bacteriophages (wild-, RGD-, and EEEE-type) were utilized as a primary building block. This sensor system was used to analyze a pattern of color change caused by a reaction between the sensor array and external substances, followed by separating the specific target substances by means of hierarchical cluster analysis. The biosensor platform could detect drug contaminants such as hormone drugs (estrogen) and antibiotics. We expect that the proposed biosensor system could be used for the development of a first-analysis kit, which would be inexpensive and easy to supply and could be applied in monitoring the environment and health care.

Indexed as

hierarchical cluster analysishigh selectivityM13 bacteriophagemulti-array sensors

Identifiers

PMID31936438
PMCPMC7023180

What OpenQuestion holds

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LicenceCC BY
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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.