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Rationally seeded computational protein design of ɑ-helical barrels
by
Petrenas, Rokas
, Borucu, Ufuk
, Woolfson, Derek N.
, Leggett, Graham. J.
, Albanese, Katherine I.
, Dawson, William M.
, Pirro, Fabio
, Naudin, Elise A.
, Weiner, Orion D.
, Oliver, Thomas A. A.
, Scott, D. Arne
in
631/92/469
/ 639/638/92/469
/ Amino Acid Sequence
/ Assemblies
/ Barrels
/ Biochemical Engineering
/ Biochemistry
/ Bioorganic Chemistry
/ Cell Biology
/ Channels
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Computational Biology - methods
/ Computer applications
/ Connectors
/ Design
/ E coli
/ Escherichia coli - genetics
/ Escherichia coli - metabolism
/ Gene expression
/ Genes
/ Helices
/ Models, Molecular
/ Peptides
/ Peptides - chemistry
/ Peptides - genetics
/ Protein Conformation, alpha-Helical
/ Protein Engineering - methods
/ Protein Folding
/ Proteins
/ Proteins - chemistry
/ Proteins - genetics
2024
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Rationally seeded computational protein design of ɑ-helical barrels
by
Petrenas, Rokas
, Borucu, Ufuk
, Woolfson, Derek N.
, Leggett, Graham. J.
, Albanese, Katherine I.
, Dawson, William M.
, Pirro, Fabio
, Naudin, Elise A.
, Weiner, Orion D.
, Oliver, Thomas A. A.
, Scott, D. Arne
in
631/92/469
/ 639/638/92/469
/ Amino Acid Sequence
/ Assemblies
/ Barrels
/ Biochemical Engineering
/ Biochemistry
/ Bioorganic Chemistry
/ Cell Biology
/ Channels
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Computational Biology - methods
/ Computer applications
/ Connectors
/ Design
/ E coli
/ Escherichia coli - genetics
/ Escherichia coli - metabolism
/ Gene expression
/ Genes
/ Helices
/ Models, Molecular
/ Peptides
/ Peptides - chemistry
/ Peptides - genetics
/ Protein Conformation, alpha-Helical
/ Protein Engineering - methods
/ Protein Folding
/ Proteins
/ Proteins - chemistry
/ Proteins - genetics
2024
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Rationally seeded computational protein design of ɑ-helical barrels
by
Petrenas, Rokas
, Borucu, Ufuk
, Woolfson, Derek N.
, Leggett, Graham. J.
, Albanese, Katherine I.
, Dawson, William M.
, Pirro, Fabio
, Naudin, Elise A.
, Weiner, Orion D.
, Oliver, Thomas A. A.
, Scott, D. Arne
in
631/92/469
/ 639/638/92/469
/ Amino Acid Sequence
/ Assemblies
/ Barrels
/ Biochemical Engineering
/ Biochemistry
/ Bioorganic Chemistry
/ Cell Biology
/ Channels
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Computational Biology - methods
/ Computer applications
/ Connectors
/ Design
/ E coli
/ Escherichia coli - genetics
/ Escherichia coli - metabolism
/ Gene expression
/ Genes
/ Helices
/ Models, Molecular
/ Peptides
/ Peptides - chemistry
/ Peptides - genetics
/ Protein Conformation, alpha-Helical
/ Protein Engineering - methods
/ Protein Folding
/ Proteins
/ Proteins - chemistry
/ Proteins - genetics
2024
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Rationally seeded computational protein design of ɑ-helical barrels
Journal Article
Rationally seeded computational protein design of ɑ-helical barrels
2024
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Overview
Computational protein design is advancing rapidly. Here we describe efficient routes starting from validated parallel and antiparallel peptide assemblies to design two families of α-helical barrel proteins with central channels that bind small molecules. Computational designs are seeded by the sequences and structures of defined de novo oligomeric barrel-forming peptides, and adjacent helices are connected by loop building. For targets with antiparallel helices, short loops are sufficient. However, targets with parallel helices require longer connectors; namely, an outer layer of helix–turn–helix–turn–helix motifs that are packed onto the barrels. Throughout these computational pipelines, residues that define open states of the barrels are maintained. This minimizes sequence sampling, accelerating the design process. For each of six targets, just two to six synthetic genes are made for expression in
Escherichia coli
. On average, 70% of these genes express to give soluble monomeric proteins that are fully characterized, including high-resolution structures for most targets that match the design models with high accuracy.
An efficient computational pipeline starting from validated peptide assemblies has been used to design two families of α-helical barrel proteins with functionalizable channels. This rationally seeded computational protein design approach delivers soluble, monomeric proteins that match the design targets accurately and with high success rates.
Publisher
Nature Publishing Group US,Nature Publishing Group
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