Cargando…
Affimer proteins are versatile and renewable affinity reagents
Molecular recognition reagents are key tools for understanding biological processes and are used universally by scientists to study protein expression, localisation and interactions. Antibodies remain the most widely used of such reagents and many show excellent performance, although some are poorly...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487212/ https://www.ncbi.nlm.nih.gov/pubmed/28654419 http://dx.doi.org/10.7554/eLife.24903 |
_version_ | 1783246418349129728 |
---|---|
author | Tiede, Christian Bedford, Robert Heseltine, Sophie J Smith, Gina Wijetunga, Imeshi Ross, Rebecca AlQallaf, Danah Roberts, Ashley PE Balls, Alexander Curd, Alistair Hughes, Ruth E Martin, Heather Needham, Sarah R Zanetti-Domingues, Laura C Sadigh, Yashar Peacock, Thomas P Tang, Anna A Gibson, Naomi Kyle, Hannah Platt, Geoffrey W Ingram, Nicola Taylor, Thomas Coletta, Louise P Manfield, Iain Knowles, Margaret Bell, Sandra Esteves, Filomena Maqbool, Azhar Prasad, Raj K Drinkhill, Mark Bon, Robin S Patel, Vikesh Goodchild, Sarah A Martin-Fernandez, Marisa Owens, Ray J Nettleship, Joanne E Webb, Michael E Harrison, Michael Lippiat, Jonathan D Ponnambalam, Sreenivasan Peckham, Michelle Smith, Alastair Ferrigno, Paul Ko Johnson, Matt McPherson, Michael J Tomlinson, Darren Charles |
author_facet | Tiede, Christian Bedford, Robert Heseltine, Sophie J Smith, Gina Wijetunga, Imeshi Ross, Rebecca AlQallaf, Danah Roberts, Ashley PE Balls, Alexander Curd, Alistair Hughes, Ruth E Martin, Heather Needham, Sarah R Zanetti-Domingues, Laura C Sadigh, Yashar Peacock, Thomas P Tang, Anna A Gibson, Naomi Kyle, Hannah Platt, Geoffrey W Ingram, Nicola Taylor, Thomas Coletta, Louise P Manfield, Iain Knowles, Margaret Bell, Sandra Esteves, Filomena Maqbool, Azhar Prasad, Raj K Drinkhill, Mark Bon, Robin S Patel, Vikesh Goodchild, Sarah A Martin-Fernandez, Marisa Owens, Ray J Nettleship, Joanne E Webb, Michael E Harrison, Michael Lippiat, Jonathan D Ponnambalam, Sreenivasan Peckham, Michelle Smith, Alastair Ferrigno, Paul Ko Johnson, Matt McPherson, Michael J Tomlinson, Darren Charles |
author_sort | Tiede, Christian |
collection | PubMed |
description | Molecular recognition reagents are key tools for understanding biological processes and are used universally by scientists to study protein expression, localisation and interactions. Antibodies remain the most widely used of such reagents and many show excellent performance, although some are poorly characterised or have stability or batch variability issues, supporting the use of alternative binding proteins as complementary reagents for many applications. Here we report on the use of Affimer proteins as research reagents. We selected 12 diverse molecular targets for Affimer selection to exemplify their use in common molecular and cellular applications including the (a) selection against various target molecules; (b) modulation of protein function in vitro and in vivo; (c) labelling of tumour antigens in mouse models; and (d) use in affinity fluorescence and super-resolution microscopy. This work shows that Affimer proteins, as is the case for other alternative binding scaffolds, represent complementary affinity reagents to antibodies for various molecular and cell biology applications. DOI: http://dx.doi.org/10.7554/eLife.24903.001 |
format | Online Article Text |
id | pubmed-5487212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54872122017-06-30 Affimer proteins are versatile and renewable affinity reagents Tiede, Christian Bedford, Robert Heseltine, Sophie J Smith, Gina Wijetunga, Imeshi Ross, Rebecca AlQallaf, Danah Roberts, Ashley PE Balls, Alexander Curd, Alistair Hughes, Ruth E Martin, Heather Needham, Sarah R Zanetti-Domingues, Laura C Sadigh, Yashar Peacock, Thomas P Tang, Anna A Gibson, Naomi Kyle, Hannah Platt, Geoffrey W Ingram, Nicola Taylor, Thomas Coletta, Louise P Manfield, Iain Knowles, Margaret Bell, Sandra Esteves, Filomena Maqbool, Azhar Prasad, Raj K Drinkhill, Mark Bon, Robin S Patel, Vikesh Goodchild, Sarah A Martin-Fernandez, Marisa Owens, Ray J Nettleship, Joanne E Webb, Michael E Harrison, Michael Lippiat, Jonathan D Ponnambalam, Sreenivasan Peckham, Michelle Smith, Alastair Ferrigno, Paul Ko Johnson, Matt McPherson, Michael J Tomlinson, Darren Charles eLife Biochemistry Molecular recognition reagents are key tools for understanding biological processes and are used universally by scientists to study protein expression, localisation and interactions. Antibodies remain the most widely used of such reagents and many show excellent performance, although some are poorly characterised or have stability or batch variability issues, supporting the use of alternative binding proteins as complementary reagents for many applications. Here we report on the use of Affimer proteins as research reagents. We selected 12 diverse molecular targets for Affimer selection to exemplify their use in common molecular and cellular applications including the (a) selection against various target molecules; (b) modulation of protein function in vitro and in vivo; (c) labelling of tumour antigens in mouse models; and (d) use in affinity fluorescence and super-resolution microscopy. This work shows that Affimer proteins, as is the case for other alternative binding scaffolds, represent complementary affinity reagents to antibodies for various molecular and cell biology applications. DOI: http://dx.doi.org/10.7554/eLife.24903.001 eLife Sciences Publications, Ltd 2017-06-27 /pmc/articles/PMC5487212/ /pubmed/28654419 http://dx.doi.org/10.7554/eLife.24903 Text en © 2017, Tiede et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Tiede, Christian Bedford, Robert Heseltine, Sophie J Smith, Gina Wijetunga, Imeshi Ross, Rebecca AlQallaf, Danah Roberts, Ashley PE Balls, Alexander Curd, Alistair Hughes, Ruth E Martin, Heather Needham, Sarah R Zanetti-Domingues, Laura C Sadigh, Yashar Peacock, Thomas P Tang, Anna A Gibson, Naomi Kyle, Hannah Platt, Geoffrey W Ingram, Nicola Taylor, Thomas Coletta, Louise P Manfield, Iain Knowles, Margaret Bell, Sandra Esteves, Filomena Maqbool, Azhar Prasad, Raj K Drinkhill, Mark Bon, Robin S Patel, Vikesh Goodchild, Sarah A Martin-Fernandez, Marisa Owens, Ray J Nettleship, Joanne E Webb, Michael E Harrison, Michael Lippiat, Jonathan D Ponnambalam, Sreenivasan Peckham, Michelle Smith, Alastair Ferrigno, Paul Ko Johnson, Matt McPherson, Michael J Tomlinson, Darren Charles Affimer proteins are versatile and renewable affinity reagents |
title | Affimer proteins are versatile and renewable affinity reagents |
title_full | Affimer proteins are versatile and renewable affinity reagents |
title_fullStr | Affimer proteins are versatile and renewable affinity reagents |
title_full_unstemmed | Affimer proteins are versatile and renewable affinity reagents |
title_short | Affimer proteins are versatile and renewable affinity reagents |
title_sort | affimer proteins are versatile and renewable affinity reagents |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487212/ https://www.ncbi.nlm.nih.gov/pubmed/28654419 http://dx.doi.org/10.7554/eLife.24903 |
work_keys_str_mv | AT tiedechristian affimerproteinsareversatileandrenewableaffinityreagents AT bedfordrobert affimerproteinsareversatileandrenewableaffinityreagents AT heseltinesophiej affimerproteinsareversatileandrenewableaffinityreagents AT smithgina affimerproteinsareversatileandrenewableaffinityreagents AT wijetungaimeshi affimerproteinsareversatileandrenewableaffinityreagents AT rossrebecca affimerproteinsareversatileandrenewableaffinityreagents AT alqallafdanah affimerproteinsareversatileandrenewableaffinityreagents AT robertsashleype affimerproteinsareversatileandrenewableaffinityreagents AT ballsalexander affimerproteinsareversatileandrenewableaffinityreagents AT curdalistair affimerproteinsareversatileandrenewableaffinityreagents AT hughesruthe affimerproteinsareversatileandrenewableaffinityreagents AT martinheather affimerproteinsareversatileandrenewableaffinityreagents AT needhamsarahr affimerproteinsareversatileandrenewableaffinityreagents AT zanettidomingueslaurac affimerproteinsareversatileandrenewableaffinityreagents AT sadighyashar affimerproteinsareversatileandrenewableaffinityreagents AT peacockthomasp affimerproteinsareversatileandrenewableaffinityreagents AT tangannaa affimerproteinsareversatileandrenewableaffinityreagents AT gibsonnaomi affimerproteinsareversatileandrenewableaffinityreagents AT kylehannah affimerproteinsareversatileandrenewableaffinityreagents AT plattgeoffreyw affimerproteinsareversatileandrenewableaffinityreagents AT ingramnicola affimerproteinsareversatileandrenewableaffinityreagents AT taylorthomas affimerproteinsareversatileandrenewableaffinityreagents AT colettalouisep affimerproteinsareversatileandrenewableaffinityreagents AT manfieldiain affimerproteinsareversatileandrenewableaffinityreagents AT knowlesmargaret affimerproteinsareversatileandrenewableaffinityreagents AT bellsandra affimerproteinsareversatileandrenewableaffinityreagents AT estevesfilomena affimerproteinsareversatileandrenewableaffinityreagents AT maqboolazhar affimerproteinsareversatileandrenewableaffinityreagents AT prasadrajk affimerproteinsareversatileandrenewableaffinityreagents AT drinkhillmark affimerproteinsareversatileandrenewableaffinityreagents AT bonrobins affimerproteinsareversatileandrenewableaffinityreagents AT patelvikesh affimerproteinsareversatileandrenewableaffinityreagents AT goodchildsaraha affimerproteinsareversatileandrenewableaffinityreagents AT martinfernandezmarisa affimerproteinsareversatileandrenewableaffinityreagents AT owensrayj affimerproteinsareversatileandrenewableaffinityreagents AT nettleshipjoannee affimerproteinsareversatileandrenewableaffinityreagents AT webbmichaele affimerproteinsareversatileandrenewableaffinityreagents AT harrisonmichael affimerproteinsareversatileandrenewableaffinityreagents AT lippiatjonathand affimerproteinsareversatileandrenewableaffinityreagents AT ponnambalamsreenivasan affimerproteinsareversatileandrenewableaffinityreagents AT peckhammichelle affimerproteinsareversatileandrenewableaffinityreagents AT smithalastair affimerproteinsareversatileandrenewableaffinityreagents AT ferrignopaulko affimerproteinsareversatileandrenewableaffinityreagents AT johnsonmatt affimerproteinsareversatileandrenewableaffinityreagents AT mcphersonmichaelj affimerproteinsareversatileandrenewableaffinityreagents AT tomlinsondarrencharles affimerproteinsareversatileandrenewableaffinityreagents |