Sagar Batra
Open and closed conformations of a sub-80 kDa Chagas vaccine candidate defined by a cryo-EM led integrative approach
Batra, Sagar; Ragan, Timothy J.; Frank, Asger M.; Kaplan, Merve; Lancey, Claudia; Assadipapari, Mahya; Ying, Cuifeng; Struwe, Weston B.; Hesketh, Emma; Barfod, Lea; Campeotto, Ivan
Authors
Timothy J. Ragan
Asger M. Frank
Merve Kaplan
Claudia Lancey
Mahya Assadipapari
Cuifeng Ying
Weston B. Struwe
Emma Hesketh
Lea Barfod
IVAN CAMPEOTTO Ivan.Campeotto@nottingham.ac.uk
Assistant Professor
Abstract
Chagas disease, caused by the protozoan parasite Trypanosoma cruzi, remains a significant global public health concern. It affects an estimated eight million individuals worldwide, with the majority remaining undiagnosed. Despite its profound health impact in both endemic and non-endemic areas, no vaccine is available, and the existing therapies are outdated, producing severe side effects.
The 80kDa prolyl oligopeptidase of Trypanosoma cruzi (TcPOP) has been recently identified as a leading candidate for Chagas vaccine development. However, its three-dimensional structure has remained elusive for almost two decades since its discovery. We report the first three-dimensional structure of TcPOP in open and closed conformation, at a resolution of 3.0 and 2.5 Angstroms respectively, determined using single-particle cryo-electron microscopy. Multiple conformations were observed and were further characterized, using plasmonic optical tweezers.
To assess the immunogenic potential of TcPOP, we immunized mice and evaluated both polyclonal and monoclonal responses against the TcPOP antigen and its homologues. The results revealed unexpected cross-reactivity across prolyl POPs from other closely related parasites, but intriguingly, not towards the human homologue.
Altogether, our findings provide critical structural insights necessary to understand the immunogenicity of TcPOP for future Chagas vaccine development and diagnostic applications.
Additionally, our integrative approach indicated that stage-tilted acquisition can yield biologically relevant information for challenging sub-80kDa proteins and could adequately resolve the cryoEM structures. Consequently, this comprehensive strategy can significantly enhance the success rate in determining the structures of proteins that present challenges in characterization.
Citation
Batra, S., Ragan, T. J., Frank, A. M., Kaplan, M., Lancey, C., Assadipapari, M., …Campeotto, I. Open and closed conformations of a sub-80 kDa Chagas vaccine candidate defined by a cryo-EM led integrative approach
Working Paper Type | Working Paper |
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Deposit Date | Mar 31, 2024 |
Publicly Available Date | Apr 9, 2024 |
Public URL | https://nottingham-repository.worktribe.com/output/33028123 |
Publisher URL | https://www.biorxiv.org/content/10.1101/2024.03.26.586384v1 |
Files
Open and closed conformations of a sub-80 kDa Chagas vaccine
(1.1 Mb)
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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