Evidence map›Paper›PMID 27548698›Full record

ArticlePloS one2016

One-Tube-Only Standardized Site-Directed Mutagenesis: An Alternative Approach to Generate Amino Acid Substitution Collections.

Janire Mingo, Asier Erramuzpe, Sandra Luna, Olaia Aurtenetxe, Laura Amo, Ibai Diez, Jan T G Schepens, Wiljan J A J Hendriks, Jesús M Cortés, Rafael Pulido

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

10 authors.

Janire MingoBiomarkers in Cancer Unit, Biocruces Health Research Institute, Barakaldo, Spain.
Asier ErramuzpeQuantitative Biomedicine Unit, Biocruces Health Research Institute, Barakaldo, Spain.
Sandra LunaBiomarkers in Cancer Unit, Biocruces Health Research Institute, Barakaldo, Spain.
Olaia AurtenetxeBiomarkers in Cancer Unit, Biocruces Health Research Institute, Barakaldo, Spain.
Laura AmoBiomarkers in Cancer Unit, Biocruces Health Research Institute, Barakaldo, Spain.
Ibai DiezQuantitative Biomedicine Unit, Biocruces Health Research Institute, Barakaldo, Spain.
Jan T G SchepensDepartment of Cell Biology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Wiljan J A J HendriksDepartment of Cell Biology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Jesús M CortésQuantitative Biomedicine Unit, Biocruces Health Research Institute, Barakaldo, Spain.
Rafael PulidoBiomarkers in Cancer Unit, Biocruces Health Research Institute, Barakaldo, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Site-directed mutagenesis (SDM) is a powerful tool to create defined collections of protein variants for experimental and clinical purposes, but effectiveness is compromised when a large number of mutations is required. We present here a one-tube-only standardized SDM approach that generates comprehensive collections of amino acid substitution variants, including scanning- and single site-multiple mutations. The approach combines unified mutagenic primer design with the mixing of multiple distinct primer pairs and/or plasmid templates to increase the yield of a single inverse-PCR mutagenesis reaction. Also, a user-friendly program for automatic design of standardized primers for Ala-scanning mutagenesis is made available. Experimental results were compared with a modeling approach together with stochastic simulation data. For single site-multiple mutagenesis purposes and for simultaneous mutagenesis in different plasmid backgrounds, combination of primer sets and/or plasmid templates in a single reaction tube yielded the distinct mutations in a stochastic fashion. For scanning mutagenesis, we found that a combination of overlapping primer sets in a single PCR reaction allowed the yield of different individual mutations, although this yield did not necessarily follow a stochastic trend. Double mutants were generated when the overlap of primer pairs was below 60%. Our results illustrate that one-tube-only SDM effectively reduces the number of reactions required in large-scale mutagenesis strategies, facilitating the generation of comprehensive collections of protein variants suitable for functional analysis.

Indexed as

Amino Acid SubstitutionMutationDNA PrimersEscherichia coliGene ExpressionHumansMutagenesis, Site-DirectedPlasmidsPolymerase Chain ReactionPTEN PhosphohydrolaseReceptor-Like Protein Tyrosine Phosphatases, Class 5SoftwareDNA PrimersPTEN PhosphohydrolasePTEN protein, humanPTPRZ1 protein, humanReceptor-Like Protein Tyrosine Phosphatases, Class 5

Identifiers

PMID27548698
PMCPMC4993582

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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.