Labelizer: systematic selection of protein residues for covalent fluorophore labeling

Attaching fluorescent dyes to biomolecules is essential for assays in biology, biochemistry, biophysics, biomedicine and imaging. A systematic approach for the selection of suitable labeling sites in macromolecules, particularly proteins, is missing. We present a quantitative strategy to identify such protein residues using a naïve Bayes classifier. Analysis of >100 proteins with ~400 successfully labeled residues allows to identify four parameters, which can rank residues via a single metric (the label score). The approach is tested and benchmarked by inspection of literature data and experiments on the expression level, degree of labelling, and success in FRET assays of different bacterial substrate binding proteins. With the paper, we provide a python package and webserver (https://labelizer.bio.lmu.de/), that performs an analysis of a pdb-structure (or model), label score calculation, and FRET assay scoring. The approach can facilitate to build up a central open-access database to continuously refine the label-site selection in proteins.

Publication Details

Journal
Technische Universität Dortmund Eldorado (Technische Universität Dortmund)
Published
2025-05-04
DOI
https://doi.org/10.17877/de290r-25534
Primary Topic
Cell Image Analysis Techniques
Type
article
Field-Weighted Citation Impact
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article

Labelizer: systematic selection of protein residues for covalent fluorophore labeling

Technische Universität Dortmund Eldorado (Technische Universität Dortmund)
Cell Image Analysis Techniques
article

Labelizer: systematic selection of protein residues for covalent fluorophore labeling

article en

Abstract

Attaching fluorescent dyes to biomolecules is essential for assays in biology, biochemistry, biophysics, biomedicine and imaging. A systematic approach for the selection of suitable labeling sites in macromolecules, particularly proteins, is missing. We present a quantitative strategy to identify such protein residues using a naïve Bayes classifier. Analysis of >100 proteins with ~400 successfully labeled residues allows to identify four parameters, which can rank residues via a single metric (the label score). The approach is tested and benchmarked by inspection of literature data and experiments on the expression level, degree of labelling, and success in FRET assays of different bacterial substrate binding proteins. With the paper, we provide a python package and webserver (https://labelizer.bio.lmu.de/), that performs an analysis of a pdb-structure (or model), label score calculation, and FRET assay scoring. The approach can facilitate to build up a central open-access database to continuously refine the label-site selection in proteins.

Technische Universität Dortmund Eldorado (Technische Universität Dortmund)
Openalex Percentile: Top 53%
Cell Image Analysis Techniques
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