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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...

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Autores principales: 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
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
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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
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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
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