Abstract
The study of biomolecular stability of proteins and lipids in extreme saline environments is critical for understanding the preservation of potential microbial biosignatures of ancient life on Earth and other planetary bodies, including Mars. In this study, we evaluate the compatibility of several analytical techniques, Nano-Differential Scanning Fluorometry (NanoDSF), Analytical Ultracentrifugation (AUC), and Differential Scanning Calorimetry (DSC) with hypersaline brine analogues of Early Earth and Early Mars conditions. Using the halophilic archaeon Halobacterium salinarum as a model, we examine the structural stability of proteins within cell envelope fragments from dead cells, focusing on their preservation potential in complex brines. The results reveal significant technical challenges in studying macromolecules in high-salinity environments, including crystallisation during DSC and NanoDSF, viscosity-related artifacts in AUC, and reduced fluorescence signals in NanoDSF due to the low tryptophan content of membrane proteins from halophilic archaea. Nevertheless, NanoDSF proved useful for analysing multi-protein systems and DSC may be applicable using new generation technology, while AUC showed limited applicability under extreme saline conditions. These findings provide crucial insights into the methodologies for studying the stability of halophilic biomolecules in brine environments and the limitations of current techniques in extreme settings.