Evidence map›Paper›PMID 37405652›Full record

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

Accessing Transient Binding Pockets by Protein Engineering and Yeast Surface Display Screening.

Jorge A Lerma Romero, Harald Kolmar

Abstract read
PubMed Publisher
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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

2 authors.

Jorge A Lerma RomeroInstitute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, Darmstadt, Germany.
Harald KolmarInstitute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, Darmstadt, Germany. Harald.Kolmar@TU-Darmstadt.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The binding pocket of some therapeutic targets can acquire multiple conformations that, to some extent, depend on the protein dynamics and the interaction with other molecules. The inability to reach the binding pocket can impose a substantial or even insurmountable barrier for the de novo identification or optimization of small-molecule ligands. Herein, we describe a protocol for the engineering of a target protein and a yeast display FACS sorting strategy to identify protein variants with a stable transient binding pocket with improved binding for a cryptic site-specific ligand. This strategy may facilitate drug discovery using the resulting protein variants with accessible binding pockets for ligand screening.

Indexed as

ProteinsSaccharomyces cerevisiaeBinding SitesDrug DiscoveryLigandsProtein BindingProtein ConformationProtein EngineeringLigandsProteinsCell cytometryProtein engineeringTransient binding pocketsYeast surface display

Identifiers

PMID37405652

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.