Loading…
Choice of fusion proteins, expression host, and analytics solves difficult‐to‐produce protein challenges in discovery research
High quality biological reagents are a prerequisite for pharmacological research. Herein a protein production screening approach, including quality assessment methods, for protein‐based discovery research is presented. Trends from 2895 expression constructs representing 253 proteins screened in mamm...
Saved in:
Published in: | Biotechnology journal 2024-01, Vol.19 (1), p.e2300162-n/a |
---|---|
Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3852-6bbdc675400bfb4b89dd1174311b7c92e58916e79b71888935bae3f348aeda933 |
---|---|
cites | cdi_FETCH-LOGICAL-c3852-6bbdc675400bfb4b89dd1174311b7c92e58916e79b71888935bae3f348aeda933 |
container_end_page | n/a |
container_issue | 1 |
container_start_page | e2300162 |
container_title | Biotechnology journal |
container_volume | 19 |
creator | Lyons‐Abbott, Sally Abramov, Ariel Chan, Chung‐leung Deer, Jen Running Fu, Guangsen Hassouneh, Wafa Koch, Tyree Misquith, Ayesha O'Neill, Jason Simon, Sandy Alexander Wolf, Anitra Yeh, Ronald Vernet, Erik |
description | High quality biological reagents are a prerequisite for pharmacological research. Herein a protein production screening approach, including quality assessment methods, for protein‐based discovery research is presented. Trends from 2895 expression constructs representing 253 proteins screened in mammalian and bacterial hosts—91% of which are successfully expressed and purified—are discussed. Mammalian expression combined with the use of solubility‐promoting fusion proteins is deemed suitable for most targets. Furthermore, cases utilizing stable cell line generation and choice of fusion protein for higher yield and quality of difficult‐to‐produce proteins (Leucine‐rich repeat‐containing G‐protein coupled receptor 4 (LGR4) and Neurturin) are presented and discussed. In the case of Neurturin, choice of fusion protein impacted the target binding 80‐fold. These results highlight the need for exploration of construct designs and careful Quality Control (QC) of difficult‐to‐produce protein reagents.
Graphical and Lay Summary
Over 2800 variants of over 250 different human proteins were expressed in bacterial and mammalian expression system. The highest success rate was found using large plasma proteins such as albumin as fusion proteins. The proteins were carefully characterized and stable cell line generated in a particular challenging case. |
doi_str_mv | 10.1002/biot.202300162 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2874270462</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2874270462</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3852-6bbdc675400bfb4b89dd1174311b7c92e58916e79b71888935bae3f348aeda933</originalsourceid><addsrcrecordid>eNqFkMtOGzEUhq0KVELolmXlJYsk9W3GnmUblRIJiQ2sR76caYyccTqeCWRX8QQ8I09Sp0nTJQsf20ff-XT0I3RJyYwSwr4YH_sZI4wTQkv2AY2oKslUcipODu9SluoMnaf0SIgoOBEf0RmXijBK1Qi9zJfRW8Cxwc2QfGzxuos9-DZNMDyvO0h_m8uY-gnWrctHh23vbcIphg0k7HzTeDuE_u33ax9zyQI3ZOVBhO1ShwDtz8zmn_PJxg10W5zdoDu7vECnjQ4JPh3uMXq4_n4_v5ne3v1YzL_eTi1XBZuWxjhbykIQYhojjKqco1QKTqmRtmJQqIqWICsjqVKq4oXRwBsulAanK87H6GrvzYv9GiD19SrvAiHoFuKQaqakYJKIkmV0tkdtF1PqoKnXnV_pbltTUu9yr3e518fc88Dng3swK3BH_F_QGaj2wJMPsH1HV39b3N3_l_8B8EGUBw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2874270462</pqid></control><display><type>article</type><title>Choice of fusion proteins, expression host, and analytics solves difficult‐to‐produce protein challenges in discovery research</title><source>Wiley</source><creator>Lyons‐Abbott, Sally ; Abramov, Ariel ; Chan, Chung‐leung ; Deer, Jen Running ; Fu, Guangsen ; Hassouneh, Wafa ; Koch, Tyree ; Misquith, Ayesha ; O'Neill, Jason ; Simon, Sandy Alexander ; Wolf, Anitra ; Yeh, Ronald ; Vernet, Erik</creator><creatorcontrib>Lyons‐Abbott, Sally ; Abramov, Ariel ; Chan, Chung‐leung ; Deer, Jen Running ; Fu, Guangsen ; Hassouneh, Wafa ; Koch, Tyree ; Misquith, Ayesha ; O'Neill, Jason ; Simon, Sandy Alexander ; Wolf, Anitra ; Yeh, Ronald ; Vernet, Erik</creatorcontrib><description>High quality biological reagents are a prerequisite for pharmacological research. Herein a protein production screening approach, including quality assessment methods, for protein‐based discovery research is presented. Trends from 2895 expression constructs representing 253 proteins screened in mammalian and bacterial hosts—91% of which are successfully expressed and purified—are discussed. Mammalian expression combined with the use of solubility‐promoting fusion proteins is deemed suitable for most targets. Furthermore, cases utilizing stable cell line generation and choice of fusion protein for higher yield and quality of difficult‐to‐produce proteins (Leucine‐rich repeat‐containing G‐protein coupled receptor 4 (LGR4) and Neurturin) are presented and discussed. In the case of Neurturin, choice of fusion protein impacted the target binding 80‐fold. These results highlight the need for exploration of construct designs and careful Quality Control (QC) of difficult‐to‐produce protein reagents.
Graphical and Lay Summary
Over 2800 variants of over 250 different human proteins were expressed in bacterial and mammalian expression system. The highest success rate was found using large plasma proteins such as albumin as fusion proteins. The proteins were carefully characterized and stable cell line generated in a particular challenging case.</description><identifier>ISSN: 1860-6768</identifier><identifier>EISSN: 1860-7314</identifier><identifier>DOI: 10.1002/biot.202300162</identifier><identifier>PMID: 37802118</identifier><language>eng</language><publisher>Germany</publisher><subject>Animals ; Cell Line ; Mammals ; Neurturin ; protein engineering ; protein expression ; protein purification ; Recombinant Fusion Proteins - genetics ; recombinant proteins</subject><ispartof>Biotechnology journal, 2024-01, Vol.19 (1), p.e2300162-n/a</ispartof><rights>2023 Wiley‐VCH GmbH.</rights><rights>2023 Wiley-VCH GmbH.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3852-6bbdc675400bfb4b89dd1174311b7c92e58916e79b71888935bae3f348aeda933</citedby><cites>FETCH-LOGICAL-c3852-6bbdc675400bfb4b89dd1174311b7c92e58916e79b71888935bae3f348aeda933</cites><orcidid>0000-0002-4175-1244</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37802118$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lyons‐Abbott, Sally</creatorcontrib><creatorcontrib>Abramov, Ariel</creatorcontrib><creatorcontrib>Chan, Chung‐leung</creatorcontrib><creatorcontrib>Deer, Jen Running</creatorcontrib><creatorcontrib>Fu, Guangsen</creatorcontrib><creatorcontrib>Hassouneh, Wafa</creatorcontrib><creatorcontrib>Koch, Tyree</creatorcontrib><creatorcontrib>Misquith, Ayesha</creatorcontrib><creatorcontrib>O'Neill, Jason</creatorcontrib><creatorcontrib>Simon, Sandy Alexander</creatorcontrib><creatorcontrib>Wolf, Anitra</creatorcontrib><creatorcontrib>Yeh, Ronald</creatorcontrib><creatorcontrib>Vernet, Erik</creatorcontrib><title>Choice of fusion proteins, expression host, and analytics solves difficult‐to‐produce protein challenges in discovery research</title><title>Biotechnology journal</title><addtitle>Biotechnol J</addtitle><description>High quality biological reagents are a prerequisite for pharmacological research. Herein a protein production screening approach, including quality assessment methods, for protein‐based discovery research is presented. Trends from 2895 expression constructs representing 253 proteins screened in mammalian and bacterial hosts—91% of which are successfully expressed and purified—are discussed. Mammalian expression combined with the use of solubility‐promoting fusion proteins is deemed suitable for most targets. Furthermore, cases utilizing stable cell line generation and choice of fusion protein for higher yield and quality of difficult‐to‐produce proteins (Leucine‐rich repeat‐containing G‐protein coupled receptor 4 (LGR4) and Neurturin) are presented and discussed. In the case of Neurturin, choice of fusion protein impacted the target binding 80‐fold. These results highlight the need for exploration of construct designs and careful Quality Control (QC) of difficult‐to‐produce protein reagents.
Graphical and Lay Summary
Over 2800 variants of over 250 different human proteins were expressed in bacterial and mammalian expression system. The highest success rate was found using large plasma proteins such as albumin as fusion proteins. The proteins were carefully characterized and stable cell line generated in a particular challenging case.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Mammals</subject><subject>Neurturin</subject><subject>protein engineering</subject><subject>protein expression</subject><subject>protein purification</subject><subject>Recombinant Fusion Proteins - genetics</subject><subject>recombinant proteins</subject><issn>1860-6768</issn><issn>1860-7314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOGzEUhq0KVELolmXlJYsk9W3GnmUblRIJiQ2sR76caYyccTqeCWRX8QQ8I09Sp0nTJQsf20ff-XT0I3RJyYwSwr4YH_sZI4wTQkv2AY2oKslUcipODu9SluoMnaf0SIgoOBEf0RmXijBK1Qi9zJfRW8Cxwc2QfGzxuos9-DZNMDyvO0h_m8uY-gnWrctHh23vbcIphg0k7HzTeDuE_u33ax9zyQI3ZOVBhO1ShwDtz8zmn_PJxg10W5zdoDu7vECnjQ4JPh3uMXq4_n4_v5ne3v1YzL_eTi1XBZuWxjhbykIQYhojjKqco1QKTqmRtmJQqIqWICsjqVKq4oXRwBsulAanK87H6GrvzYv9GiD19SrvAiHoFuKQaqakYJKIkmV0tkdtF1PqoKnXnV_pbltTUu9yr3e518fc88Dng3swK3BH_F_QGaj2wJMPsH1HV39b3N3_l_8B8EGUBw</recordid><startdate>202401</startdate><enddate>202401</enddate><creator>Lyons‐Abbott, Sally</creator><creator>Abramov, Ariel</creator><creator>Chan, Chung‐leung</creator><creator>Deer, Jen Running</creator><creator>Fu, Guangsen</creator><creator>Hassouneh, Wafa</creator><creator>Koch, Tyree</creator><creator>Misquith, Ayesha</creator><creator>O'Neill, Jason</creator><creator>Simon, Sandy Alexander</creator><creator>Wolf, Anitra</creator><creator>Yeh, Ronald</creator><creator>Vernet, Erik</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4175-1244</orcidid></search><sort><creationdate>202401</creationdate><title>Choice of fusion proteins, expression host, and analytics solves difficult‐to‐produce protein challenges in discovery research</title><author>Lyons‐Abbott, Sally ; Abramov, Ariel ; Chan, Chung‐leung ; Deer, Jen Running ; Fu, Guangsen ; Hassouneh, Wafa ; Koch, Tyree ; Misquith, Ayesha ; O'Neill, Jason ; Simon, Sandy Alexander ; Wolf, Anitra ; Yeh, Ronald ; Vernet, Erik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3852-6bbdc675400bfb4b89dd1174311b7c92e58916e79b71888935bae3f348aeda933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Mammals</topic><topic>Neurturin</topic><topic>protein engineering</topic><topic>protein expression</topic><topic>protein purification</topic><topic>Recombinant Fusion Proteins - genetics</topic><topic>recombinant proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lyons‐Abbott, Sally</creatorcontrib><creatorcontrib>Abramov, Ariel</creatorcontrib><creatorcontrib>Chan, Chung‐leung</creatorcontrib><creatorcontrib>Deer, Jen Running</creatorcontrib><creatorcontrib>Fu, Guangsen</creatorcontrib><creatorcontrib>Hassouneh, Wafa</creatorcontrib><creatorcontrib>Koch, Tyree</creatorcontrib><creatorcontrib>Misquith, Ayesha</creatorcontrib><creatorcontrib>O'Neill, Jason</creatorcontrib><creatorcontrib>Simon, Sandy Alexander</creatorcontrib><creatorcontrib>Wolf, Anitra</creatorcontrib><creatorcontrib>Yeh, Ronald</creatorcontrib><creatorcontrib>Vernet, Erik</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lyons‐Abbott, Sally</au><au>Abramov, Ariel</au><au>Chan, Chung‐leung</au><au>Deer, Jen Running</au><au>Fu, Guangsen</au><au>Hassouneh, Wafa</au><au>Koch, Tyree</au><au>Misquith, Ayesha</au><au>O'Neill, Jason</au><au>Simon, Sandy Alexander</au><au>Wolf, Anitra</au><au>Yeh, Ronald</au><au>Vernet, Erik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Choice of fusion proteins, expression host, and analytics solves difficult‐to‐produce protein challenges in discovery research</atitle><jtitle>Biotechnology journal</jtitle><addtitle>Biotechnol J</addtitle><date>2024-01</date><risdate>2024</risdate><volume>19</volume><issue>1</issue><spage>e2300162</spage><epage>n/a</epage><pages>e2300162-n/a</pages><issn>1860-6768</issn><eissn>1860-7314</eissn><abstract>High quality biological reagents are a prerequisite for pharmacological research. Herein a protein production screening approach, including quality assessment methods, for protein‐based discovery research is presented. Trends from 2895 expression constructs representing 253 proteins screened in mammalian and bacterial hosts—91% of which are successfully expressed and purified—are discussed. Mammalian expression combined with the use of solubility‐promoting fusion proteins is deemed suitable for most targets. Furthermore, cases utilizing stable cell line generation and choice of fusion protein for higher yield and quality of difficult‐to‐produce proteins (Leucine‐rich repeat‐containing G‐protein coupled receptor 4 (LGR4) and Neurturin) are presented and discussed. In the case of Neurturin, choice of fusion protein impacted the target binding 80‐fold. These results highlight the need for exploration of construct designs and careful Quality Control (QC) of difficult‐to‐produce protein reagents.
Graphical and Lay Summary
Over 2800 variants of over 250 different human proteins were expressed in bacterial and mammalian expression system. The highest success rate was found using large plasma proteins such as albumin as fusion proteins. The proteins were carefully characterized and stable cell line generated in a particular challenging case.</abstract><cop>Germany</cop><pmid>37802118</pmid><doi>10.1002/biot.202300162</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-4175-1244</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1860-6768 |
ispartof | Biotechnology journal, 2024-01, Vol.19 (1), p.e2300162-n/a |
issn | 1860-6768 1860-7314 |
language | eng |
recordid | cdi_proquest_miscellaneous_2874270462 |
source | Wiley |
subjects | Animals Cell Line Mammals Neurturin protein engineering protein expression protein purification Recombinant Fusion Proteins - genetics recombinant proteins |
title | Choice of fusion proteins, expression host, and analytics solves difficult‐to‐produce protein challenges in discovery research |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T20%3A32%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Choice%20of%20fusion%20proteins,%20expression%20host,%20and%20analytics%20solves%20difficult%E2%80%90to%E2%80%90produce%20protein%20challenges%20in%20discovery%20research&rft.jtitle=Biotechnology%20journal&rft.au=Lyons%E2%80%90Abbott,%20Sally&rft.date=2024-01&rft.volume=19&rft.issue=1&rft.spage=e2300162&rft.epage=n/a&rft.pages=e2300162-n/a&rft.issn=1860-6768&rft.eissn=1860-7314&rft_id=info:doi/10.1002/biot.202300162&rft_dat=%3Cproquest_cross%3E2874270462%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3852-6bbdc675400bfb4b89dd1174311b7c92e58916e79b71888935bae3f348aeda933%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2874270462&rft_id=info:pmid/37802118&rfr_iscdi=true |