The production of a genus-specific recombinant antibody (scFv) using a recombinant potyvirus protease

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  • Technische Universität Braunschweig
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OriginalspracheEnglisch
Seiten (von - bis)225-233
FachzeitschriftJournal of Virological Methods
Jahrgang106
Ausgabenummer2
PublikationsstatusVeröffentlicht - 2002

Abstract

A single chain variable fragment antibody (scFv; anti-NIa scFv102) was selected from a synthetic human antibody library by using a NIa protease of Plum pox virus (PPV) as an antigen, which was expressed in bacteria. The NIa protease forms the nuclear inclusion body A and acts as the major protease in the cleavage of the viral polyprotein into functional proteins. The NIa protein was detected with anti-NIa scFv102 after expression in Escherichia coli cells as well as from PPV-infected Nicotiana benthamiana plants. Furthermore, the scFv102 has the ability to identify not only PPV from infected plants but also can detect other infections with members of the potyviruses. Nineteen different potyviruses were recognized by the scFv102 in various infected plants tested through dot blot assays. Therefore, the antibody scFv102 has the potential of becoming a general tool to detect potyvirus infections in different plant species. ?? 2002 Published by Elsevier Science B.V.

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The production of a genus-specific recombinant antibody (scFv) using a recombinant potyvirus protease. / Reinard, Thomas; Maiß, Edgar; Hust, Michael.
in: Journal of Virological Methods, Jahrgang 106, Nr. 2, 2002, S. 225-233.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "The production of a genus-specific recombinant antibody (scFv) using a recombinant potyvirus protease",
abstract = "A single chain variable fragment antibody (scFv; anti-NIa scFv102) was selected from a synthetic human antibody library by using a NIa protease of Plum pox virus (PPV) as an antigen, which was expressed in bacteria. The NIa protease forms the nuclear inclusion body A and acts as the major protease in the cleavage of the viral polyprotein into functional proteins. The NIa protein was detected with anti-NIa scFv102 after expression in Escherichia coli cells as well as from PPV-infected Nicotiana benthamiana plants. Furthermore, the scFv102 has the ability to identify not only PPV from infected plants but also can detect other infections with members of the potyviruses. Nineteen different potyviruses were recognized by the scFv102 in various infected plants tested through dot blot assays. Therefore, the antibody scFv102 has the potential of becoming a general tool to detect potyvirus infections in different plant species. ?? 2002 Published by Elsevier Science B.V.",
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note = "Funding information: The generous gift of virus-infected plants from Dr. Vetten, BBA Braunschweig, Germany, is gratefully acknowledged. We thank Imdadul Hoque for helpful comments on the manuscript. This work is supported by the Ministry of Science and Culture (MWK) of the state Lower Saxony.",
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AU - Reinard, Thomas

AU - Maiß, Edgar

AU - Hust, Michael

N1 - Funding information: The generous gift of virus-infected plants from Dr. Vetten, BBA Braunschweig, Germany, is gratefully acknowledged. We thank Imdadul Hoque for helpful comments on the manuscript. This work is supported by the Ministry of Science and Culture (MWK) of the state Lower Saxony.

PY - 2002

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AB - A single chain variable fragment antibody (scFv; anti-NIa scFv102) was selected from a synthetic human antibody library by using a NIa protease of Plum pox virus (PPV) as an antigen, which was expressed in bacteria. The NIa protease forms the nuclear inclusion body A and acts as the major protease in the cleavage of the viral polyprotein into functional proteins. The NIa protein was detected with anti-NIa scFv102 after expression in Escherichia coli cells as well as from PPV-infected Nicotiana benthamiana plants. Furthermore, the scFv102 has the ability to identify not only PPV from infected plants but also can detect other infections with members of the potyviruses. Nineteen different potyviruses were recognized by the scFv102 in various infected plants tested through dot blot assays. Therefore, the antibody scFv102 has the potential of becoming a general tool to detect potyvirus infections in different plant species. ?? 2002 Published by Elsevier Science B.V.

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DO - 10.1016/S0166-0934(02)00166-0

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