MutateX: an automated pipeline for in silico saturation mutagenesis of protein structures and structural ensembles. Issue 3 (22nd March 2022)
- Record Type:
- Journal Article
- Title:
- MutateX: an automated pipeline for in silico saturation mutagenesis of protein structures and structural ensembles. Issue 3 (22nd March 2022)
- Main Title:
- MutateX: an automated pipeline for in silico saturation mutagenesis of protein structures and structural ensembles
- Authors:
- Tiberti, Matteo
Terkelsen, Thilde
Degn, Kristine
Beltrame, Ludovica
Cremers, Tycho Canter
da Piedade, Isabelle
Di Marco, Miriam
Maiani, Emiliano
Papaleo, Elena - Abstract:
- Abstract: Mutations, which result in amino acid substitutions, influence the stability of proteins and their binding to biomolecules. A molecular understanding of the effects of protein mutations is both of biotechnological and medical relevance. Empirical free energy functions that quickly estimate the free energy change upon mutation (ΔΔ G ) can be exploited for systematic screenings of proteins and protein complexes. In silico saturation mutagenesis can guide the design of new experiments or rationalize the consequences of known mutations. Often software such as FoldX, while fast and reliable, lack the necessary automation features to apply them in a high-throughput manner. We introduce MutateX, a software to automate the prediction of ΔΔ G s associated with the systematic mutation of each residue within a protein, or protein complex to all other possible residue types, using the FoldX energy function. MutateX also supports ΔΔ G calculations over protein ensembles, upon post-translational modifications and in multimeric assemblies. At the heart of MutateX lies an automated pipeline engine that handles input preparation, parallelization and outputs publication-ready figures. We illustrate the MutateX protocol applied to different case studies. The results of the high-throughput scan provided by our tools can help in different applications, such as the analysis of disease-associated mutations, to complement experimental deep mutational scans, or assist the design ofAbstract: Mutations, which result in amino acid substitutions, influence the stability of proteins and their binding to biomolecules. A molecular understanding of the effects of protein mutations is both of biotechnological and medical relevance. Empirical free energy functions that quickly estimate the free energy change upon mutation (ΔΔ G ) can be exploited for systematic screenings of proteins and protein complexes. In silico saturation mutagenesis can guide the design of new experiments or rationalize the consequences of known mutations. Often software such as FoldX, while fast and reliable, lack the necessary automation features to apply them in a high-throughput manner. We introduce MutateX, a software to automate the prediction of ΔΔ G s associated with the systematic mutation of each residue within a protein, or protein complex to all other possible residue types, using the FoldX energy function. MutateX also supports ΔΔ G calculations over protein ensembles, upon post-translational modifications and in multimeric assemblies. At the heart of MutateX lies an automated pipeline engine that handles input preparation, parallelization and outputs publication-ready figures. We illustrate the MutateX protocol applied to different case studies. The results of the high-throughput scan provided by our tools can help in different applications, such as the analysis of disease-associated mutations, to complement experimental deep mutational scans, or assist the design of variants for industrial applications. MutateX is a collection of Python tools that relies on open-source libraries. It is available free of charge under the GNU General Public License from https://github.com/ELELAB/mutatex . … (more)
- Is Part Of:
- Briefings in bioinformatics. Volume 23:Issue 3(2022)
- Journal:
- Briefings in bioinformatics
- Issue:
- Volume 23:Issue 3(2022)
- Issue Display:
- Volume 23, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 23
- Issue:
- 3
- Issue Sort Value:
- 2022-0023-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-03-22
- Subjects:
- free energy -- mutations -- post-translational modifications -- structural ensembles -- binding -- stability
Genetics -- Data processing -- Periodicals
Molecular biology -- Data processing -- Periodicals
Genomes -- Data processing -- Periodicals
572.80285 - Journal URLs:
- http://bib.oxfordjournals.org ↗
http://www.oxfordjournals.org/content?genre=journal&issn=1477-4054 ↗
http://ukcatalogue.oup.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1093/bib/bbac074 ↗
- Languages:
- English
- ISSNs:
- 1467-5463
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2283.958363
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21549.xml