Evidence map›Paper›PMID 37405660›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

SUMO: In Silico Sequence Assessment Using Multiple Optimization Parameters.

Andreas Evers, Shipra Malhotra, Wolf-Guido Bolick, Ahmad Najafian, Maria Borisovska, Shira Warszawski, Yves Fomekong Nanfack, Daniel Kuhn, Friedrich Rippmann, Alejandro Crespo and 1 more

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. 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

11 authors.

Andreas EversComputational Chemistry & Biologics (CCB), Merck Healthcare KGaA, Darmstadt, Germany. Andreas.Evers@merckgroup.com.ORCID 0000-0003-4643-1941
Shipra MalhotraComputational Chemistry & Biologics (CCB), EMD Serono, Billerica, MA, USA.
Wolf-Guido BolickGinkgo Analytics GmbH, Hamburg, Germany.
Ahmad NajafianComputational Chemistry & Biologics (CCB), EMD Serono, Billerica, MA, USA.
Maria BorisovskaComputational Chemistry & Biologics (CCB), EMD Serono, Billerica, MA, USA.
Shira WarszawskiComputational Chemistry & Biologics, Merck KGaA, Yavne, Israel.
Yves Fomekong NanfackComputational Chemistry & Biologics (CCB), EMD Serono, Billerica, MA, USA.
Daniel KuhnComputational Chemistry & Biologics (CCB), Merck Healthcare KGaA, Darmstadt, Germany.
Friedrich RippmannComputational Chemistry & Biologics (CCB), Merck Healthcare KGaA, Darmstadt, Germany.
Alejandro CrespoComputational Chemistry & Biologics (CCB), EMD Serono, Billerica, MA, USA.
Vanita SoodComputational Chemistry & Biologics (CCB), EMD Serono, Billerica, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To select the most promising screening hits from antibody and VHH display campaigns for subsequent in-depth profiling and optimization, it is highly desirable to assess and select sequences on properties beyond only their binding signals from the sorting process. In addition, developability risk criteria, sequence diversity, and the anticipated complexity for sequence optimization are relevant attributes for hit selection and optimization. Here, we describe an approach for the in silico developability assessment of antibody and VHH sequences. This method not only allows for ranking and filtering multiple sequences with regard to their predicted developability properties and diversity, but also visualizes relevant sequence and structural features of potentially problematic regions and thereby provides rationales and starting points for multi-parameter sequence optimization.

Indexed as

AntibodiesAntibodiesAntibodyDevelopabilityHumanizationImmunogenicityIn silico sequence assessmentMulti-parameter optimizationProtein engineeringVHH (variable domain of the heavy chain of heavy chain-only antibodies)

Identifiers

What OpenQuestion holds

Textmetadata
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.