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Enzymatic synthesis of antibody-human serum albumin conjugate for targeted drug delivery using tyrosinase from Agaricus bisporus

Highly specific targeted drug delivery devices can be obtained with antibody-human serum albumin (mAb-HSA) conjugates. However, their conventional production involves several reaction steps including chemical modification and activation of both proteins followed by cross-linking often involving toxi...

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Published in:RSC advances 2013-01, Vol.3 (5), p.1460-1467
Main Authors: Rollett, Alexandra, Thallinger, Barbara, Ohradanova-Repic, Anna, Machacek, Christian, Walenta, Evelyn, Paulo, Artur Cavaco, Birner-Gruenberger, Ruth, Bogner-Strauss, Juliane G., Stockinger, Hannes, Guebitz, G. M.
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cited_by cdi_FETCH-LOGICAL-c391t-be98948eda728183ddbf85488bd40e27f649c4e5c120e7fb3f93a9de983599e33
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creator Rollett, Alexandra
Thallinger, Barbara
Ohradanova-Repic, Anna
Machacek, Christian
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Bogner-Strauss, Juliane G.
Stockinger, Hannes
Guebitz, G. M.
description Highly specific targeted drug delivery devices can be obtained with antibody-human serum albumin (mAb-HSA) conjugates. However, their conventional production involves several reaction steps including chemical modification and activation of both proteins followed by cross-linking often involving toxic chemicals. Here, we describe the enzymatic synthesis of mAb-HSA conjugates for targeted drug delivery devices using tyrosinase from Agaricus bisporus under mild reaction conditions (pH 6.8, 25 [degree]C). Reaction conditions were optimized by using fluorescence labeled HSA to facilitate SDS-PAGE analysis with fluorescence scanning. Enzymatic cross-linking in the presence of natural low molecular weight phenolic compounds (e.g. caffeic acid) resulted in reaction products in the molecular weight range of [similar]216 kDa, corresponding to mAb-HSA conjugates. The composition of the conjugates was confirmed with tryptic digestion followed by LC-MS/MS analysis of the resulting peptide fragments. Successful binding of mAb-HSA conjugates (in contrast to free HSA) to MHC II molecules, located on antigen-presenting cells, was demonstrated by both ELISA and flow cytometry analysis. This work has received funding from the European Union Seventh Framework Programme (FP7/2007-2013) under grant agreement NMP4-LA-2009-228827 NANOFOL and FWF, DK: Metabolic and Cardiovascular Disease: W1226-B18. We thank Tamara Reiter, Graz University of Technology for technical support with SEC; Exbio from the Czech Republic for providing the mAbs and Britta Obrist, Medical University of Graz and the Austrian Centre of Industrial Biotechnology, for technical assistance with LC-MS/MS analysis.
doi_str_mv 10.1039/c2ra22560c
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subjects Agaricus
Albumin
Science & Technology
title Enzymatic synthesis of antibody-human serum albumin conjugate for targeted drug delivery using tyrosinase from Agaricus bisporus
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