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. 2020 Nov 17;10:19997. doi: 10.1038/s41598-020-77095-x

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© The Author(s) 2020

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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Binding kinetics of TRAIL-ATNC with TRAIL receptor. (A,B) Surface plasmon resonance analysis for the binding kinetics of TRAIL and TRAIL-ATNC with TRAIL receptor (DR5). The concentrations of TRAIL (25–400 nM) and TRAIL-ATNC (0.52–8.33 nM) were injected to DR5 coated dextran-coated chips. (C) Representative fluorescence images of TRAIL, TRAIL-ATNC, and wild type ferritin (Wt FtH) bound to A549 cells, showing efficient cell binding of TRAIL and TRAIL-ATNC. A549 cells were treated with 50 nM of each protein for 1 h at 4 ℃ and immunostained with anti-His tag antibodies (red). Nuclei were counterstained with DAPI (blue). Scale bars: 30 µm.