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. 2022 Aug 4;5:785. doi: 10.1038/s42003-022-03767-1

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© The Author(s) 2022

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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Fig. 2 — a Overview of site-specific N-linked glycan processing in ebolavirus GPΔTM from HEK293 and S2 cells as determined by LC-MS/MS. The glycans were classified by HexNAc content as truncated, paucimannose, oligomannose, hybrid or complex. Shown is the average of a duplicate experiment. b Pseudomodel of EBOV GP (as in Fig. 1), with glycans colored by main class (oligomannose, hybrid, complex) as observed in HEK293 cells.