Mann Lab (@mannlab.bsky.social)

Characterizing the ZenoTOF 8600 in collaboration @sciex.bsky.social . Scanning DIA on a compact platform — ~10K protein groups in bulk to single-cell proteomics & Parkinson's-relevant phosphosite detection with complementary CID & EAD fragmentation. biorxiv.org/content/10.64898/2026.03.12.711261v1

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Scanning DIA on the ZenoTOF 8600 system enables ultra-sensitive and quantitative proteomics from single cells to post-translational modifications in a compact platform Mass spectrometry-based proteomics increasingly demands platforms that combine quantitative rigor with the discovery capabilities of accurate mass systems. Here we present the ZenoTOF 8600 system, a compact mass spectrometry system that integrates enhanced ion capture and transmission optics with an optical detection system, Zeno trap-enhanced MS/MS, electron-activated dissociation, and scanning quadrupole data-independent acquisition (ZT Scan DIA). We show that ZT Scan DIA outperforms conventional variable-window DIA (Zeno SWATH DIA) in both identifications and quantitative reproducibility, and demonstrate the platform's versatility across proteomics applications: thousands of protein groups from bulk samples at up to 500 samples per day, single-cell proteomics yielding up to 4,700 proteins, accurate ratio recovery in mixed-species quantitative benchmarks, low-attomole targeted quantitation, and detection of disease-relevant phosphorylation in a Parkinson's disease cellular model using complementary CID and EAD fragmentation. The instrument's compact footprint makes it attractive for settings where both analytical breadth and operational robustness are required. ### Competing Interest Statement B.L., Y.L.B., N. B., I.B., J.C., A.C., G.I., K.T., T.T., B.S., and J.C.-P. are employees of SCIEX. M.M. is an indirect investor in Evosep Biosystems. The remaining authors declare no competing interests. https://biorxiv.org/content/10.64898/2026.03.12.711261v1