Evidence map›Paper›PMID 31796769›Full record

ArticleScientific reports2019

Transmembrane signaling on a protocell: Creation of receptor-enzyme chimeras for immunodetection of specific antibodies and antigens.

Jiulong Su, Tetsuya Kitaguchi, Yuki Ohmuro-Matsuyama, Theresa Seah, Farid J Ghadessy, Shawn Hoon, Hiroshi Ueda

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Membrane-Associated Biomolecules for Synthetic Cell Signalling.Chembiochem : a European journal of chemical biology · 2026
    Review
  2. 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

7 authors at 4 institutions in 3 countries.

Jiulong SuGraduate School of Life Science and Technology, Tokyo Institute of Technology, 4259-R1-18 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.
Tetsuya KitaguchiLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, 4259-R1-18 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.
Yuki Ohmuro-MatsuyamaLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, 4259-R1-18 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan.
Theresa SeahMolecular Engineering Laboratory, Biomedical Sciences Institutes, Agency for Science Technology and Research (A*STAR), 61 Biopolis Drive, Singapore, 138673, Singapore.
Farid J Ghadessyp53 Laboratory, Agency for Science Technology and Research (A*STAR), 8A Biomedical Grove, Singapore, 138673, Singapore.
Shawn HoonMolecular Engineering Laboratory, Biomedical Sciences Institutes, Agency for Science Technology and Research (A*STAR), 61 Biopolis Drive, Singapore, 138673, Singapore.
Hiroshi UedaLaboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, 4259-R1-18 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa, 226-8503, Japan. ueda@res.titech.ac.jp.
Agency for Science, Technology and Research · SGTokyo Institute of Technology · JPInnovative Research (United States) · USLife Science Institute · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is known that digital counting of fluorescent signals generated in many small compartments can significantly improve the detection sensitivity of the enzyme-linked immunosorbent assay (ELISA). However, the reported digital ELISA systems need extensive washing steps to remove background signal, which hampers their performance. To tackle this problem, we developed a vesicle (Protocell) array wherein binding of an external protein analyte is coupled to signal amplification and intra-vesicular fluorescence readout. We chose β-glucuronidase (GUS) as a reporter enzyme as its function requires assembly of four subunits through dimerization of a pair of dimers that can be inhibited by a set of interface mutations. Using a thermostabilized GUS mutant IV-5, we screened out an interface mutant (M516K, F517W) to create IV5

Indexed as

AntibodiesAntigensChimeraEnzyme-Linked Immunosorbent AssayGlucuronidaseHumansMembrane ProteinsSignal TransductionTrastuzumabAntibodiesAntigensGlucuronidaseMembrane ProteinsTrastuzumab

Identifiers

PMID31796769
PMCPMC6890649
OpenAlexW2993143574

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.