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. 2017 Nov 3;7:14476. doi: 10.1038/s41598-017-15251-6

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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HSA Peptide 40 Binding to Monoclonal Antibodies Bevacizumab, Rituximab, and Trastuzumab Kinetic Binding Parameters Determined by Biacore-SPR: A peptide library of human serum albumin (HSA) was screened via Biacore over immobilized antibodies bevacizumab, rituximab, and trastuzumab. Antibodies were immobilized via amine coupling and peptides were run at pM-uM concentration ranges. (a) HSA Peptide 40 binding curves (180 second association period, 1200 second dissociation period) against all three antibodies and the negative control antibody pembrolizumab. (b) Binding kinetics were determined via Biacore Evaluation Software analysis of SPR sensograms.