Evidence map›Paper›PMID 42400843›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Methods for the In Vitro Selection of Protein and Peptide Libraries Using mRNA Display.

Colin M Leaf, Pearl Qi, Richard W Roberts, Terry T Takahashi

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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

4 authors.

Colin M Leaf *Department of Chemistry, University of Southern California, Los Angeles, CA, 90089, USA.
Pearl Qi *Mork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, CA, 90089, USA.
Richard W RobertsDepartment of Chemistry, University of Southern California, Los Angeles, CA, 90089, USA. richrob@usc.edu.
Terry T TakahashiDepartment of Chemistry, University of Southern California, Los Angeles, CA, 90089, USA. tttakaha@usc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

mRNA display is a powerful in vitro selection technique that enables the discovery of peptide and protein ligands from libraries exceeding 10 trillion unique sequences. The technique allows for exquisite control over binding stringency and specificity, and it is highly amenable to high-throughput ligand profiling and integration with machine learning approaches. Here, we describe general methods for performing mRNA display selections.

Indexed as

Peptide LibraryPeptidesProteinsRNA, MessengerCombinatorial Chemistry TechniquesDirected Molecular EvolutionLigandsProtein EngineeringLigandsPeptide LibraryPeptidesProteinsRNA, MessengerCombinatorial chemistryDirected evolutionIn vitro selectionLigand discoverymRNA displayProtein engineeringRNA-protein fusion

Identifiers

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.