Isolation and Characterization of Nanobodies against a Zinc-Transporting P-Type ATPase
P-type ATPases form a large and ubiquitous superfamily of ion and lipid transporters that use ATP (adenosine triphosphate) to carry out their function. The IB subclass (P<sub>IB</sub>-ATPases) allows flux of heavy metals and are key players in metal detoxification, critical for human hea...
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doaj-9fad5b04d85d482dba3006440dabe9e92020-11-25T01:30:37ZengMDPI AGAntibodies2073-44682018-11-01743910.3390/antib7040039antib7040039Isolation and Characterization of Nanobodies against a Zinc-Transporting P-Type ATPaseElena Longhin0Christina Grønberg1Qiaoxia Hu2Annette Susanne Duelli3Kasper Røjkjær Andersen4Nick Stub Laursen5Pontus Gourdon6Department of Biomedical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200 Copenhagen, DenmarkDepartment of Biomedical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200 Copenhagen, DenmarkDepartment of Biomedical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200 Copenhagen, DenmarkDepartment of Biomedical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200 Copenhagen, DenmarkDepartment of Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej 10c, DK-8000 Aarhus C, DenmarkDepartment of Molecular Biology and Genetics, Aarhus University, Gustav Wieds Vej 10c, DK-8000 Aarhus C, DenmarkDepartment of Biomedical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200 Copenhagen, DenmarkP-type ATPases form a large and ubiquitous superfamily of ion and lipid transporters that use ATP (adenosine triphosphate) to carry out their function. The IB subclass (P<sub>IB</sub>-ATPases) allows flux of heavy metals and are key players in metal detoxification, critical for human health, crops, and survival of pathogens. Nevertheless, P<sub>IB</sub>-ATPases remain poorly understood at a molecular level. In this study, nanobodies (Nbs) are selected against the zinc-transporting P<sub>IB</sub>-ATPase ZntA from <i>Shigella sonnei</i> (SsZntA), aiming at developing tools to assist the characterization of the structure and function of this class of transporters. We identify six different Nbs that bind detergent stabilized SsZntA. We further assess the effect of the Nbs on the catalytic function of SsZntA, and find that five nanobodies associate without affecting the function, while one nanobody significantly reduces the ATPase activity. This study paves the way for more refined mechanistical and structural studies of zinc-transporting P<sub>IB</sub>-ATPases.https://www.mdpi.com/2073-4468/7/4/39P-type ATPasenanobodyllamaZinc-transportZinc-transporting P-ATPaseZntA |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Elena Longhin Christina Grønberg Qiaoxia Hu Annette Susanne Duelli Kasper Røjkjær Andersen Nick Stub Laursen Pontus Gourdon |
spellingShingle |
Elena Longhin Christina Grønberg Qiaoxia Hu Annette Susanne Duelli Kasper Røjkjær Andersen Nick Stub Laursen Pontus Gourdon Isolation and Characterization of Nanobodies against a Zinc-Transporting P-Type ATPase Antibodies P-type ATPase nanobody llama Zinc-transport Zinc-transporting P-ATPase ZntA |
author_facet |
Elena Longhin Christina Grønberg Qiaoxia Hu Annette Susanne Duelli Kasper Røjkjær Andersen Nick Stub Laursen Pontus Gourdon |
author_sort |
Elena Longhin |
title |
Isolation and Characterization of Nanobodies against a Zinc-Transporting P-Type ATPase |
title_short |
Isolation and Characterization of Nanobodies against a Zinc-Transporting P-Type ATPase |
title_full |
Isolation and Characterization of Nanobodies against a Zinc-Transporting P-Type ATPase |
title_fullStr |
Isolation and Characterization of Nanobodies against a Zinc-Transporting P-Type ATPase |
title_full_unstemmed |
Isolation and Characterization of Nanobodies against a Zinc-Transporting P-Type ATPase |
title_sort |
isolation and characterization of nanobodies against a zinc-transporting p-type atpase |
publisher |
MDPI AG |
series |
Antibodies |
issn |
2073-4468 |
publishDate |
2018-11-01 |
description |
P-type ATPases form a large and ubiquitous superfamily of ion and lipid transporters that use ATP (adenosine triphosphate) to carry out their function. The IB subclass (P<sub>IB</sub>-ATPases) allows flux of heavy metals and are key players in metal detoxification, critical for human health, crops, and survival of pathogens. Nevertheless, P<sub>IB</sub>-ATPases remain poorly understood at a molecular level. In this study, nanobodies (Nbs) are selected against the zinc-transporting P<sub>IB</sub>-ATPase ZntA from <i>Shigella sonnei</i> (SsZntA), aiming at developing tools to assist the characterization of the structure and function of this class of transporters. We identify six different Nbs that bind detergent stabilized SsZntA. We further assess the effect of the Nbs on the catalytic function of SsZntA, and find that five nanobodies associate without affecting the function, while one nanobody significantly reduces the ATPase activity. This study paves the way for more refined mechanistical and structural studies of zinc-transporting P<sub>IB</sub>-ATPases. |
topic |
P-type ATPase nanobody llama Zinc-transport Zinc-transporting P-ATPase ZntA |
url |
https://www.mdpi.com/2073-4468/7/4/39 |
work_keys_str_mv |
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