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In Silico Engineering of Synthetic Binding Proteins from Random Amino Acid Sequences

Authors :
Daniel Burnside
Andrew Schoenrock
Houman Moteshareie
Mohsen Hooshyar
Prabh Basra
Maryam Hajikarimlou
Kevin Dick
Brad Barnes
Tom Kazmirchuk
Matthew Jessulat
Sylvain Pitre
Bahram Samanfar
Mohan Babu
James R. Green
Alex Wong
Frank Dehne
Kyle K. Biggar
Ashkan Golshani
Source :
iScience, Vol 11, Iss , Pp 375-387 (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

Summary: Synthetic proteins with high affinity and selectivity for a protein target can be used as research tools, biomarkers, and pharmacological agents, but few methods exist to design such proteins de novo. To this end, the In-Silico Protein Synthesizer (InSiPS) was developed to design synthetic binding proteins (SBPs) that bind pre-determined targets while minimizing off-target interactions. InSiPS is a genetic algorithm that refines a pool of random sequences over hundreds of generations of mutation and selection to produce SBPs with pre-specified binding characteristics. As a proof of concept, we design SBPs against three yeast proteins and demonstrate binding and functional inhibition of two of three targets in vivo. Peptide SPOT arrays confirm binding sites, and a permutation array demonstrates target specificity. Our foundational approach will support the field of de novo design of small binding polypeptide motifs and has robust applicability while offering potential advantages over the limited number of techniques currently available. : Biological Sciences; Bioinformatics; Protein Family Determination Subject Areas: Biological Sciences, Bioinformatics, Protein Family Determination

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
25890042
Volume :
11
Issue :
375-387
Database :
Directory of Open Access Journals
Journal :
iScience
Publication Type :
Academic Journal
Accession number :
edsdoj.ba2fc64ebce64d13a9bc7d5d6d6d626e
Document Type :
article
Full Text :
https://doi.org/10.1016/j.isci.2018.11.038