Improved lipid analysis to inform future therapeutic strategies

Lead Research Organisation: University of Nottingham
Department Name: Sch of Pharmacy

Abstract

Antimicrobial resistance (AMR) threatens to rival cancer in mortality and financial burden by 2050. Mycobacterial infections are the primary bacterial cause of global morbidity and mortality (2 million deaths annually), costing $12 billion, with lipids implicated in AMR1. Medulloblastoma is the most common malignant child brain tumour, with various phospholipids implicated in tumour metastastasis2. Because lipids are indicative of disease/progression and impact therapeutic strategies/success it is imperative to have sensitive methods of detection and identification directly from biological samples.
Surface-sampling MS approaches offer the benefit of direct analysis and imaging; recent advances in instrumentation allow coupling to high resolution (trapping) mass analysers (HRMS), offering high accurate mass analysis3,4, aiding identification. Complementary approaches will be utilised; secondary ion MS (SIMS), ambient pressure (AP) matrix-assisted laser desorption/ionisation (MALDI) and liquid extraction surface analysis (LESA).
Lipid analysis is complicated by the formation of (naturally occurring) adducts ([M+H]+, [M+Na]+, [M+K]+), decreasing sensitivity and complicating assignments. Salt additives have been shown to afford improvements in sensitivity, decrease spectral complexity and identification via MALDI and LESA5,6. MALDI matrix enhancement can also improve SIMS (ME-SIMS)7, and hasn't been investigated via OrbiSIMS. This project will deliver sensitive analytical methods for the direct detection and identification of lipids implicated in disease/infection.

Publications

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Studentship Projects

Project Reference Relationship Related To Start End Student Name
EP/T517902/1 01/10/2020 30/09/2025
2679337 Studentship EP/T517902/1 01/04/2022 30/09/2025 Sidrah Rahman