Cargando…

Droplet Microfluidics-Enabled High-Throughput Screening for Protein Engineering

Protein engineering—the process of developing useful or valuable proteins—has successfully created a wide range of proteins tailored to specific agricultural, industrial, and biomedical applications. Protein engineering may rely on rational techniques informed by structural models, phylogenic inform...

Descripción completa

Detalles Bibliográficos
Autores principales: Weng, Lindong, Spoonamore, James E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915371/
https://www.ncbi.nlm.nih.gov/pubmed/31671786
http://dx.doi.org/10.3390/mi10110734
_version_ 1783480000428638208
author Weng, Lindong
Spoonamore, James E.
author_facet Weng, Lindong
Spoonamore, James E.
author_sort Weng, Lindong
collection PubMed
description Protein engineering—the process of developing useful or valuable proteins—has successfully created a wide range of proteins tailored to specific agricultural, industrial, and biomedical applications. Protein engineering may rely on rational techniques informed by structural models, phylogenic information, or computational methods or it may rely upon random techniques such as chemical mutation, DNA shuffling, error prone polymerase chain reaction (PCR), etc. The increasing capabilities of rational protein design coupled to the rapid production of large variant libraries have seriously challenged the capacity of traditional screening and selection techniques. Similarly, random approaches based on directed evolution, which relies on the Darwinian principles of mutation and selection to steer proteins toward desired traits, also requires the screening of very large libraries of mutants to be truly effective. For either rational or random approaches, the highest possible screening throughput facilitates efficient protein engineering strategies. In the last decade, high-throughput screening (HTS) for protein engineering has been leveraging the emerging technologies of droplet microfluidics. Droplet microfluidics, featuring controlled formation and manipulation of nano- to femtoliter droplets of one fluid phase in another, has presented a new paradigm for screening, providing increased throughput, reduced reagent volume, and scalability. We review here the recent droplet microfluidics-based HTS systems developed for protein engineering, particularly directed evolution. The current review can also serve as a tutorial guide for protein engineers and molecular biologists who need a droplet microfluidics-based HTS system for their specific applications but may not have prior knowledge about microfluidics. In the end, several challenges and opportunities are identified to motivate the continued innovation of microfluidics with implications for protein engineering.
format Online
Article
Text
id pubmed-6915371
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-69153712019-12-24 Droplet Microfluidics-Enabled High-Throughput Screening for Protein Engineering Weng, Lindong Spoonamore, James E. Micromachines (Basel) Review Protein engineering—the process of developing useful or valuable proteins—has successfully created a wide range of proteins tailored to specific agricultural, industrial, and biomedical applications. Protein engineering may rely on rational techniques informed by structural models, phylogenic information, or computational methods or it may rely upon random techniques such as chemical mutation, DNA shuffling, error prone polymerase chain reaction (PCR), etc. The increasing capabilities of rational protein design coupled to the rapid production of large variant libraries have seriously challenged the capacity of traditional screening and selection techniques. Similarly, random approaches based on directed evolution, which relies on the Darwinian principles of mutation and selection to steer proteins toward desired traits, also requires the screening of very large libraries of mutants to be truly effective. For either rational or random approaches, the highest possible screening throughput facilitates efficient protein engineering strategies. In the last decade, high-throughput screening (HTS) for protein engineering has been leveraging the emerging technologies of droplet microfluidics. Droplet microfluidics, featuring controlled formation and manipulation of nano- to femtoliter droplets of one fluid phase in another, has presented a new paradigm for screening, providing increased throughput, reduced reagent volume, and scalability. We review here the recent droplet microfluidics-based HTS systems developed for protein engineering, particularly directed evolution. The current review can also serve as a tutorial guide for protein engineers and molecular biologists who need a droplet microfluidics-based HTS system for their specific applications but may not have prior knowledge about microfluidics. In the end, several challenges and opportunities are identified to motivate the continued innovation of microfluidics with implications for protein engineering. MDPI 2019-10-29 /pmc/articles/PMC6915371/ /pubmed/31671786 http://dx.doi.org/10.3390/mi10110734 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Weng, Lindong
Spoonamore, James E.
Droplet Microfluidics-Enabled High-Throughput Screening for Protein Engineering
title Droplet Microfluidics-Enabled High-Throughput Screening for Protein Engineering
title_full Droplet Microfluidics-Enabled High-Throughput Screening for Protein Engineering
title_fullStr Droplet Microfluidics-Enabled High-Throughput Screening for Protein Engineering
title_full_unstemmed Droplet Microfluidics-Enabled High-Throughput Screening for Protein Engineering
title_short Droplet Microfluidics-Enabled High-Throughput Screening for Protein Engineering
title_sort droplet microfluidics-enabled high-throughput screening for protein engineering
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915371/
https://www.ncbi.nlm.nih.gov/pubmed/31671786
http://dx.doi.org/10.3390/mi10110734
work_keys_str_mv AT wenglindong dropletmicrofluidicsenabledhighthroughputscreeningforproteinengineering
AT spoonamorejamese dropletmicrofluidicsenabledhighthroughputscreeningforproteinengineering