Evidence map›Paper›PMID 26895405›Full record

ArticlePloS one2016

Next-Generation Sequencing of a Single Domain Antibody Repertoire Reveals Quality of Phage Display Selected Candidates.

Kendrick B Turner, Jennifer Naciri, Jinny L Liu, George P Anderson, Ellen R Goldman, Dan Zabetakis

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 39 citations in OpenAlex.

  1. mAbs · 2026
    Article
  2. Article
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  5. Article
  6. Application of Deep Sequencing in Phage Display.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
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  12. 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

6 authors at 3 institutions in 1 country.

Kendrick B TurnerAmerican Society for Engineering Education, Postdoctoral Fellow at the US Naval Research Laboratory, Washington, DC, United States of America.
Jennifer NaciriAmerican Society for Engineering Education, Science and Engineering Apprenticeship Participant at US Naval Research Laboratory, Washington, DC, United States of America.
Jinny L LiuCenter for Bio/molecular Science and Engineering, US Naval Research Laboratory, Washington, DC, United States of America.
George P AndersonCenter for Bio/molecular Science and Engineering, US Naval Research Laboratory, Washington, DC, United States of America.
Ellen R GoldmanCenter for Bio/molecular Science and Engineering, US Naval Research Laboratory, Washington, DC, United States of America.
Dan ZabetakisCenter for Bio/molecular Science and Engineering, US Naval Research Laboratory, Washington, DC, United States of America.
Naval Research Laboratory Center for Bio/Molecular Science and EngineeringAmerican Society For Engineering Education · USUnited States Naval Research Laboratory · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next-Generation Sequencing and bioinformatics are powerful tools for analyzing the large number of DNA sequences present in an immune library. In this work, we constructed a cDNA library of single domain antibodies from a llama immunized with staphylococcal enterotoxin B. The resulting library was sequenced, resulting in approximately 8.5 million sequences with 5.4 million representing intact, useful sequences. The sequenced library was interrogated using sequences of known SEB-binding single domain antibodies from the library obtained through phage display panning methods in a previous study. New antibodies were identified, produced, and characterized, and were shown to have affinities and melting temperatures comparable to those obtained by traditional panning methods. This demonstrates the utility of using NGS as a complementary tool to phage-displayed biopanning as a means for rapidly obtaining additional antibodies from an immune library. It also shows that phage display, using a library of high diversity, is able to select high quality antibodies even when they are low in frequency.

Indexed as

Cell Surface Display TechniquesHigh-Throughput Nucleotide SequencingAmino Acid SequenceAntibody AffinityCloning, MolecularGene DosageGene ExpressionGene LibraryHumansMolecular Sequence DataPeptide LibraryPhylogenyProtein BindingProtein StabilitySequence AlignmentSingle-Domain AntibodiesPeptide LibrarySingle-Domain Antibodies

Identifiers

PMID26895405
PMCPMC4760936
OpenAlexW2283012379

What OpenQuestion holds

Textmetadata
LicenceCC0
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.