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. 2019 Aug 15;10:3686. doi: 10.1038/s41467-019-11642-7

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© The Author(s) 2019

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. 1 — Characterization of liposome–protein complexes. Zeta-potential (Zp, panel a) and hydrodynamic diameter (D_H, panel b) of cationic DOTAP (red), neutral DOPC (green), and anionic DOPG (blue) liposomes as functions of human plasma (HP) concentration. For clarity, size of DOPC-HP and DOPG-HP complexes are reported also in the inset of panel b. c Synchrotron small angle X-ray scattering patterns of liposome–protein complexes as a function HP concentration. The results are given as mean ± standard deviation of three replicates