Evidence map›Paper›PMID 26847261›Full record

ArticleRNA (New York, N.Y.)2016

A high-throughput pipeline for the production of synthetic antibodies for analysis of ribonucleoprotein complexes.

Hong Na, John D Laver, Jouhyun Jeon, Fateh Singh, Kristin Ancevicius, Yujie Fan, Wen Xi Cao, Kun Nie, Zhenglin Yang, Hua Luo and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2016. 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
2.4field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Regulation of theRNA (New York, N.Y.) · 2024
    Article
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  12. Article
  13. Taking Stock of theGenetics · 2017
    Review
  14. 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

17 authors at 1 institution in 1 country.

Hong NaDonnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1.
John D LaverDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Jouhyun JeonDonnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1.
Fateh SinghDonnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1.
Kristin AnceviciusDepartment of Biology, University of Toronto at Mississauga, Mississauga, Ontario, Canada L5L 1C6 Department of Cell and Systems Biology, University of Toronto at Mississauga, Mississauga, Ontario, Canada L5L 1C6.
Yujie FanDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Wen Xi CaoDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Kun NieDonnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1 Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Zhenglin YangDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Hua LuoDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Miranda WangDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8 Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada M5G 0A4.
Olivia RisslandDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8 Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada M5G 0A4.
J Timothy WestwoodDepartment of Biology, University of Toronto at Mississauga, Mississauga, Ontario, Canada L5L 1C6 Department of Cell and Systems Biology, University of Toronto at Mississauga, Mississauga, Ontario, Canada L5L 1C6.
Philip M KimDonnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1 Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8 Department of Computer Science, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Craig A SmibertDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8 Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Howard D LipshitzDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Sachdev S SidhuDonnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1 Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
University of Toronto · CA

Funding

Canadian Institutes of Health Research MOP-14409Canadian Institutes of Health Research MOP-93725
6 · The paper itself

Abstract

Post-transcriptional regulation of mRNAs plays an essential role in the control of gene expression. mRNAs are regulated in ribonucleoprotein (RNP) complexes by RNA-binding proteins (RBPs) along with associated protein and noncoding RNA (ncRNA) cofactors. A global understanding of post-transcriptional control in any cell type requires identification of the components of all of its RNP complexes. We have previously shown that these complexes can be purified by immunoprecipitation using anti-RBP synthetic antibodies produced by phage display. To develop the large number of synthetic antibodies required for a global analysis of RNP complex composition, we have established a pipeline that combines (i) a computationally aided strategy for design of antigens located outside of annotated domains, (ii) high-throughput antigen expression and purification in Escherichia coli, and (iii) high-throughput antibody selection and screening. Using this pipeline, we have produced 279 antibodies against 61 different protein components of Drosophila melanogaster RNPs. Together with those produced in our low-throughput efforts, we have a panel of 311 antibodies for 67 RNP complex proteins. Tests of a subset of our antibodies demonstrated that 89% immunoprecipitate their endogenous target from embryo lysate. This panel of antibodies will serve as a resource for global studies of RNP complexes in Drosophila. Furthermore, our high-throughput pipeline permits efficient production of synthetic antibodies against any large set of proteins.

Indexed as

Amino Acid SequenceAnimalsAntibodiesAntigensBlotting, WesternComplementarity Determining RegionsDrosophila melanogasterDrosophila ProteinsEnzyme-Linked Immunosorbent AssayEscherichia coliImmunoprecipitationMolecular Sequence DataRecombinant ProteinsRibonucleoproteinsAntibodiesAntigensComplementarity Determining RegionsDrosophila ProteinsRecombinant ProteinsRibonucleoproteinsFabphage displayribonucleoprotein complexRNA-binding proteinsynthetic antibody

Identifiers

PMID26847261
PMCPMC4793217
OpenAlexW2262611560

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.