Evidence map›Paper›PMID 40067620›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Cell-Type-Specific Protein Metabolic Labeling and Identification Using the Methionine Subrogate ANL in Cells Expressing a Mutant Methionyl-tRNA Synthetase.

Rodrigo Alvarez-Pardo, Ella Doron-Mandel, Hector Albert-Gascó, Cristina Olmedo Salinas, Marko Jovanovic, Beatriz Alvarez-Castelao

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Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rodrigo Alvarez-Pardo *Department of Biochemistry and Molecular Biology, Veterinary School, Complutense University of Madrid, Madrid, Spain.
Ella Doron-Mandel *Department of Biological Sciences, Columbia University, New York, NY, USA.
Hector Albert-GascóCambridge Institute of Science, Altos Labs, Great Abington, UK.
Cristina Olmedo SalinasDepartment of Biochemistry and Molecular Biology, Veterinary School, Complutense University of Madrid, Madrid, Spain.
Marko JovanovicDepartment of Biological Sciences, Columbia University, New York, NY, USA.
Beatriz Alvarez-CastelaoDepartment of Biochemistry and Molecular Biology, Veterinary School, Complutense University of Madrid, Madrid, Spain. balvar03@ucm.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The study of protein homeostasis in vivo is crucial for our understanding of the functions of cells and organisms. However, complex organisms, such as mammals, are built from heterogeneous tissues and cell-types. These cell-types are often specialized and react in different ways to the same physiological or pathological stimulus. Therefore, a major challenge in proteomics is the identification of proteomes and their behavior in a cell-type-specific manner. In this protocol, we describe a technique to label, enrich, and identify proteins from specific cell types. This technique is based on the expression of a mutant methionyl-tRNA synthetase (MetRS*) for incorporation of a bioorthogonal analog of methionine (ANL) into proteins. ANL can be subsequently bound to an alkyne by click-chemistry, which is used as a bait for protein purification followed by mass spectrometry identification.

Indexed as

MethionineMethionine-tRNA LigaseProteomicsAnimalsClick ChemistryHumansMass SpectrometryMutationProteomeMethionineMethionine-tRNA LigaseProteomeAzidonorleucine (ANL)Mass spectrometry (MS)Methionine-tRNA transferase (MetRS*, MARS)Noncanonical amino acids (NCAA)Protein degradationProtein homeostasisProtein synthesis

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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.