Evidence map›Paper›PMID 41620495›Full record

ArticleCommunications biology2026

Characterising nanobody developability to improve therapeutic design using the Therapeutic Nanobody Profiler.

Gemma L Gordon, João Gervasio, Colby Souders, Charlotte M Deane

Abstract read
In one paragraph

Article in Communications biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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  6. Review
  7. Efficient generation of epitope-targetedbioRxiv : the preprint server for biology · 2025
    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

4 authors.

Gemma L GordonDepartment of Statistics, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-8259-9111
João GervasioDepartment of Statistics, University of Oxford, Oxford, UK.
Colby SoudersTwist Bioscience, South San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-3700-4844
Charlotte M DeaneDepartment of Statistics, University of Oxford, Oxford, UK. deane@stats.ox.ac.uk.ORCID http://orcid.org/0000-0003-1388-2252

Funding

RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/S024093/1
6 · The paper itself

Abstract

Developability optimisation is an important step for successful biotherapeutic design. For monoclonal antibodies, developability is relatively well characterised. However, progress for novel biotherapeutics such as nanobodies is more limited. Differences in structural features between antibodies and nanobodies render current antibody computational methods unsuitable for direct application to nanobodies. Following the principles of the Therapeutic Antibody Profiler (TAP), we have built the Therapeutic Nanobody Profiler (TNP), an open-source computational tool for characterising nanobody developability. Tailored specifically for nanobodies, it accounts for their unique properties compared to conventional antibodies for more efficient development of this novel therapeutic format. We calibrate TNP metrics using the 36 currently available sequences from clinical-stage nanobody-based drugs. We also collected experimental developability data for 108 nanobodies expressed as IgG constructs and examine how these results are related to the TNP guidelines. TNP is available as a web application at opig.stats.ox.ac.uk/webapps/tnp.

Indexed as

Computational BiologyDrug DesignSingle-Domain AntibodiesSoftwareAnimalsAntibodies, MonoclonalHumansAntibodies, MonoclonalSingle-Domain Antibodies

Identifiers

PMID41620495
PMCPMC12963540

What OpenQuestion holds

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LicenceCC BY
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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.