Native Ambient Mass Spectrometry Enables Analysis of Intact Endogenous Protein Assemblies up to 145 kDa Directly from Tissue
journal contributionposted on 2022-03-31, 23:43 authored by Oliver J. Hale, James W. Hughes, Emma K. Sisley, Helen J. Cooper
Untargeted label-free interrogation of proteins in their functional form directly from their physiological environment promises to transform life sciences research by providing unprecedented insight into their transient interactions with other biomolecules and xenobiotics. Native ambient mass spectrometry (NAMS) shows great potential for the structural analysis of endogenous protein assemblies directly from tissues; however, to date, this has been limited to assemblies of low molecular weight (<20 kDa) or very high abundance (hemoglobin tetramer in blood vessels, RidA homotrimer in kidney cortex tissues). The present work constitutes a step change for NAMS of protein assemblies: we demonstrate the detection and identification of a range of intact endogenous protein assemblies with various stoichiometries (dimer, trimer, and tetramer) from a range of tissue types (brain, kidney, liver) by the use of multiple NAMS techniques. Crucially, we demonstrate a greater than twofold increase in accessible molecular weight (up to 145 kDa). In addition, spatial distributions of protein assemblies up to 94 kDa were mapped in brain and kidney by nanospray desorption electrospray ionization (nano-DESI) mass spectrometry imaging.
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shows great potentialproviding unprecedented insightpresent work constitutesphysiological environment promisesmass spectrometry imagingfunctional form directlyaccessible molecular weight145 kda directly145 kda ).tissue untargeted labelmultiple nams techniques94 kdatissue typesvarious stoichiometriestwofold increasetransient interactionsstructural analysisstep changespatial distributionsrida homotrimerhigh abundancefree interrogationblood vessels