{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Hale OJ"],"funding":["Advantage West Midlands","Biotechnology and Biological Sciences Research Council","Engineering and Physical Sciences Research Council"],"pagination":["146-152"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11697349"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["36(1)"],"pubmed_abstract":["Native mass spectrometry analysis of proteins directly from tissues can be performed by using nanospray-desorption electrospray ionization (nano-DESI). Typically, supplementary collisional activation is essential to decluster protein complex ions from solvent, salt, detergent, and lipid clusters that comprise the ion beam. As an alternative, we have implemented declustering by infrared (IR) photoactivation on a linear ion trap mass spectrometer equipped with a CO<sub>2</sub> laser (λ = 10.6 μm). The prototype system demonstrates declustering of intact protein complex ions up to approximately 50 kDa in molecular weight that were sampled directly from brain and eye lens tissues by nano-DESI. For example, signals for different metal binding states of hSOD1<sup>G93A</sup> homodimers (approxima"],"journal":["Journal of the American Society for Mass Spectrometry"],"pubmed_title":["Infrared Photoactivation Enables nano-DESI MS of Protein Complexes in Tissue on a Linear Ion Trap Mass Spectrometer."],"pmcid":["PMC11697349"],"funding_grant_id":["BB/S019456/1","EP/S002979/1"],"pubmed_authors":["Cooper HJ","Hale OJ","Mize TH"],"additional_accession":[]},"is_claimable":false,"name":"Infrared Photoactivation Enables nano-DESI MS of Protein Complexes in Tissue on a Linear Ion Trap Mass Spectrometer.","description":"Native mass spectrometry analysis of proteins directly from tissues can be performed by using nanospray-desorption electrospray ionization (nano-DESI). Typically, supplementary collisional activation is essential to decluster protein complex ions from solvent, salt, detergent, and lipid clusters that comprise the ion beam. As an alternative, we have implemented declustering by infrared (IR) photoactivation on a linear ion trap mass spectrometer equipped with a CO<sub>2</sub> laser (λ = 10.6 μm). The prototype system demonstrates declustering of intact protein complex ions up to approximately 50 kDa in molecular weight that were sampled directly from brain and eye lens tissues by nano-DESI. For example, signals for different metal binding states of hSOD1<sup>G93A</sup> homodimers (approxima","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Jan","modification":"2026-06-02T08:00:18.026Z","creation":"2025-04-04T13:41:19.036Z"},"accession":"S-EPMC11697349","cross_references":{"pubmed":["39604167"],"doi":["10.1021/jasms.4c00377"]}}