Evidence map›Paper›PMID 32151188›Full record

ArticlemAbs

Intein mediated high throughput screening for bispecific antibodies.

Tim Hofmann, Johannes Schmidt, Elke Ciesielski, Stefan Becker, Thomas Rysiok, Mark Schütte, Lars Toleikis, Harald Kolmar, Achim Doerner

Open access · goldAbstract read
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-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

17 citing papers in PubMed, 29 citations in OpenAlex.

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  12. Toward Drug-Like Multispecific Antibodies by Design.International journal of molecular sciences · 2020
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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

9 authors at 3 institutions in 2 countries.

Tim HofmannInstitute for Organic Chemistry and Biochemistry, Technische Universität Darmstadt, Darmstadt, Germany.
Johannes SchmidtCompound Logistic & Bioassay Automation, Merck KGaA, Darmstadt, Germany.
Elke CiesielskiProtein Engineering and Antibody Technologies, Merck KGaA, Darmstadt, Germany.
Stefan BeckerProtein Engineering and Antibody Technologies, Merck KGaA, Darmstadt, Germany.
Thomas RysiokProtein Engineering and Antibody Technologies, Merck KGaA, Darmstadt, Germany.
Mark SchütteGlobal Innovation and Alliance Management, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riß, Germany.
Lars ToleikisProtein Engineering and Antibody Technologies, Merck KGaA, Darmstadt, Germany.
Harald KolmarInstitute for Organic Chemistry and Biochemistry, Technische Universität Darmstadt, Darmstadt, Germany.
Achim DoernerProtein Engineering and Antibody Technologies, Merck KGaA, Darmstadt, Germany.
Merck (Germany) · DEBoehringer Ingelheim (Australia) · AUTechnical University of Darmstadt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bispecific antibodies comprise extremely diverse architectures enabling complex modes of action, such as effector cell recruitment or conditional target modulation via dual targeting, not conveyed by monospecific antibodies. In recent years, research on bispecific therapeutics has substantially grown. However, evaluation of binding moiety combinations often leads to undesired prolonged development times. While high throughput screening for small molecules and classical antibodies has evolved into a mature discipline in the pharmaceutical industry, dual-targeting antibody screening methodologies lack the ability to fully evaluate the tremendous number of possible combinations and cover only a limited portion of the combinatorial screening space. Here, we propose a novel combinatorial screening approach for bispecific IgG-like antibodies to extenuate screening limitations in industrial scale, expanding the limiting screening space. Harnessing the ability of a protein trans-splicing reaction by the split intein

Indexed as

InteinsAnimalsAntibodies, BispecificHigh-Throughput Screening AssaysHumansProtein EngineeringAntibodies, Bispecificantibodyantibody discoveryautomationbispecific antibodyHigh throughput Screeningsplit inteins

Identifiers

PMID32151188
PMCPMC7153837
OpenAlexW3009318087

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.