Evidence map›Paper›PMID 24860558›Full record

ArticleFrontiers in microbiology2014

Wheat germ cell-free system-based production of hemagglutinin-neuraminidase glycoprotein of human parainfluenza virus type 3 for generation and characterization of monoclonal antibody.

Satoko Matsunaga, Shiho Kawakami, Izumi Matsuo, Akiko Okayama, Hiroyuki Tsukagoshi, Ayumi Kudoh, Yuki Matsushima, Hideaki Shimizu, Nobuhiko Okabe, Hisashi Hirano and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
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

15 citing papers in PubMed, 19 citations in OpenAlex.

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  6. Review
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  8. Article
  9. Cell-Free Protein Synthesis: A Promising Option for Future Drug Development.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2020
    Review
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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

13 authors at 3 institutions in 2 countries.

Satoko MatsunagaDepartment of Microbiology, Yokohama City University School of Medicine Kanagawa, Japan.
Shiho KawakamiDepartment of Microbiology, Yokohama City University School of Medicine Kanagawa, Japan.
Izumi MatsuoDepartment of Microbiology, Yokohama City University School of Medicine Kanagawa, Japan.
Akiko OkayamaProteome Analysis Center, Yokohama City University School of Medicine Kanagawa, Japan.
Hiroyuki TsukagoshiGunma Prefectural Institute of Public Health and Environmental Sciences Gunma, Japan.
Ayumi KudohDepartment of Microbiology, Yokohama City University School of Medicine Kanagawa, Japan.
Yuki MatsushimaKawasaki City Health and Safety Research Center Kanagawa, Japan.
Hideaki ShimizuKawasaki City Health and Safety Research Center Kanagawa, Japan.
Nobuhiko OkabeKawasaki City Health and Safety Research Center Kanagawa, Japan.
Hisashi HiranoProteome Analysis Center, Yokohama City University School of Medicine Kanagawa, Japan.
Naoki YamamotoDepartment of Microbiology, Yong Loo Lin School of Medicine, National University of Singapore Singapore.
Hirokazu KimuraInfectious Disease Surveillance Center, National Institute of Infectious Diseases Tokyo, Japan.
Akihide RyoDepartment of Microbiology, Yokohama City University School of Medicine Kanagawa, Japan.
Yokohama City University · JPNational Institute of Infectious Diseases · JPNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human parainfluenza virus 3 (HPIV3) commonly causes respiratory disorders in infants and young children. Monoclonal antibodies (MAbs) have been produced to several components of HPIV3 and commercially available. However, the utility of these antibodies for several immunological and proteomic assays for understanding the nature of HPIV3 infection remain to be characterized. Herein, we report the development and characterization of MAbs against hemagglutinin-neuraminidase (HN) of HPIV3. A recombinant full-length HPIV3-HN was successfully synthesized using the wheat-germ cell-free protein production system. After immunization and cell fusion, 36 mouse hybridomas producing MAbs to HPIV3-HN were established. The MAbs obtained were fully characterized using ELISA, immunoblotting, and immunofluorescent analyses. Of the MAbs tested, single clone was found to be applicable in both flow cytometry and immunoprecipitation procedures. By utilizing the antibody, we identified HPIV3-HN binding host proteins via immunoprecipitation-based mass spectrometry analysis. The newly-developed MAbs could thus be a valuable tool for the study of HPIV3 infection as well as the several diagnostic tests of this virus.

Indexed as

cell-free protein synthesishuman parainfluenza virus 3monoclonal antibodyproteomics

Identifiers

PMID24860558
PMCPMC4026691
OpenAlexW2078545379

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.