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. 2023 May 27;20:9. doi: 10.1186/s12977-023-00624-9

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© The Author(s) 2023

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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — Neutralization of bNAb-depleted B41 PV by bNAbs. The extent of neutralization (%) is plotted as a function of bNAb concentration (μg/ml). PV was first incubated with Sepharose beads covalently conjugated with bNAbs PGT145 or PGT151 or mock-conjugated (see color-coded legend). The unbound virions were then tested for neutralization by the NAbs indicated in each diagram in a TZM-bl neutralization assay. The extent of neutralization (%) is plotted as a function of bNAb concentration (μg/ml), so that potencies rise as curves are shifted from right to left