Evidence map›Paper›PMID 36827414›Full record

ArticlePloS one2023

Direct selection of functional fluorescent-protein antibody fusions by yeast display.

Nileena Velappan, Fortunato Ferrara, Sara D'Angelo, Devin Close, Leslie Naranjo, Madeline R Bolding, Sarah C Mozden, Camille B Troup, Donna K McCullough, Analyssa Gomez and 2 more

Abstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Nileena VelappanBioscience Division, Los Alamos National Laboratory, Los Alamos, NM, United States of America.
Fortunato FerraraSpecifica Inc., Santa Fe, NM, United States of America.ORCID 0000-0002-4615-035X
Sara D'AngeloSpecifica Inc., Santa Fe, NM, United States of America.
Devin CloseArup Laboratories, Salt Lake City, UT, United States of America.
Leslie NaranjoSpecifica Inc., Santa Fe, NM, United States of America.
Madeline R BoldingBioscience Division, Los Alamos National Laboratory, Los Alamos, NM, United States of America.ORCID 0000-0002-8157-2531
Sarah C MozdenBioscience Division, Los Alamos National Laboratory, Los Alamos, NM, United States of America.ORCID 0000-0002-0879-9860
Camille B TroupCarterra Inc., Salt Lake City, UT, United States of America.
Donna K McCulloughMicrobiology Department, University of Tennessee, Knoxville, TN, United States of America.
Analyssa GomezBioscience Division, Los Alamos National Laboratory, Los Alamos, NM, United States of America.
Marijo KedgeBioscience Division, Los Alamos National Laboratory, Los Alamos, NM, United States of America.
Andrew R M BradburySpecifica Inc., Santa Fe, NM, United States of America.ORCID 0000-0002-5567-8172

Funding

UNM TRAININGP50GM085273 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI WANDINGER-NESS, ANGELA · 2009 to 2018
$26.1M
NIGMS NIH HHS P50 GM085273
6 · The paper itself

Abstract

Antibodies are important reagents for research, diagnostics, and therapeutics. Many examples of chimeric proteins combining the specific target recognition of antibodies with complementing functionalities such as fluorescence, toxicity or enzymatic activity have been described. However, antibodies selected solely on the basis of their binding specificities are not necessarily ideal candidates for the construction of chimeras. Here, we describe a high throughput method based on yeast display to directly select antibodies most suitable for conversion to fluorescent chimera. A library of scFv binders was converted to a fluorescent chimeric form, by cloning thermal green protein into the linker between VH and VL, and directly selecting for both binding and fluorescent functionality. This allowed us to directly identify antibodies functional in the single chain TGP format, that manifest higher protein expression, easier protein purification, and one-step binding assays.

Indexed as

Saccharomyces cerevisiaeSingle-Chain AntibodiesAntibodies, MonoclonalFluorescent Antibody TechniquePeptide LibraryAntibodies, MonoclonalPeptide LibrarySingle-Chain Antibodies

Identifiers

PMID36827414
PMCPMC9956592

What OpenQuestion holds

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Registered trials

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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.