#secretomics
Check out our work that aims to decipher Cryptococcus neoformans on an global scale. 4300 knockout strains, 142 genetic screens, 6 in depth follow up stories (too many to summarize here, but rach is cool!). AlphaFold, AP-MS, microscopy, secretomics, mice, machine learning and more.
October 24, 2024 at 4:34 AM
In #ScienceSignaling, researchers dive into the protein secretome and decrypt how peritoneal dialysis can trigger fibrosis and damage blood vessels, providing a resource that could inform efforts to limit toxicity from this lifesaving therapy. https://scim.ag/4eLt4Iv
Deep secretome analysis reveals the effects of LiCl on fibroangiogenic remodeling in coculture and mouse models of peritoneal dialysis
Secretomics uncovers cell-cell signaling networks in tissue remodeling induced by peritoneal dialysis.
scim.ag
April 29, 2026 at 3:00 PM
Thank you for visiting us at #HUPO2025! We appreciated all the conversations and look forward to meeting you again in 2026! #Mag_Net_HP expanding applications from deep #plasmaproteomics to #urinaryproteomics and #secretomics!
November 18, 2025 at 10:08 AM
Presenting my poster about Comparative Secretomics on Symbiodiniaceae TODAY at #ISME20
If interested in the secreted proteins from the algae which potentially function during symbiosis establishment, come to PS3.20.244
August 20, 2026 at 12:41 AM
(BioRxiv All) Plate-based ISD-SPE enables dual proteome-secretome concentration-response profiling of TLR signalling in iPSC-derived macrophages: Protein secretion represents a key functional output of cellular signalling, capturing dynamic responses to stimulation and… #BioRxiv #MassSpecRSS
Plate-based ISD-SPE enables dual proteome-secretome concentration-response profiling of TLR signalling in iPSC-derived macrophages
Protein secretion represents a key functional output of cellular signalling, capturing dynamic responses to stimulation and pharmacological perturbation that shape immune behaviour. In macrophages, activation of Toll-like receptors (TLRs) drives tightly regulated secretion programmes that mediate inflammatory responses and provide a biologically meaningful readout of pathway activity. Whilst mass spectrometry (MS)-based secretomics enables unbiased profiling of these processes, broader application in drug discovery remains constrained by sample preparation workflows that limit scalability. Here, we describe a plate-based in-solution digestion and solid-phase extraction (ISD-SPE) workflow that enables 96-well processing of conditioned media for integrated proteome and secretome analysis from the same sample well. Benchmarking against a precipitation-based approach demonstrated comparable proteomic depth with improved quantitative reproducibility and robust performance across multiple plates. Coupled with dia-PASEF acquisition, this workflow enabled in-depth profiling of macrophage responses to TLR activation, resolving receptor-specific secretory programmes following TLR3, TLR4 and TLR7/8 activation. Extension of the approach to concentration-response studies enabled quantitative characterisation of pharmacological perturbation across intracellular and extracellular protein landscapes, revealing both shared and compartment-specific responses to TLR inhibition, as well as differences in apparent potency linked to secretion dynamics. Together, this workflow provides a scalable strategy for integrated analysis of intracellular signalling and downstream protein secretion, enabling systems-level characterisation of inflammatory responses and compound mechanisms of action.
dlvr.it
July 22, 2026 at 4:02 AM
We performed quantitative top-down secretomics on senescent, proliferating and quiescent cells to identify senescence-specific proteoforms. We used a combination of ToPIC suite (for IDs) and Biopharma Finder (for the areas of mass features) and combined the outputs for proteoform quant. 2/n
November 19, 2025 at 11:20 AM
We inferred transcription factor and kinase activities using #DecoupleR tinyurl.com/decouple-R, integrated them w/ the secretomics data and generated mechanistic hypotheses related to transcriptional events modulating fibrotic progression using #COSMOS tinyurl.com/cosmos-R
June 27, 2025 at 1:29 PM
We profile fibrotic progression in response to #TGFb by quantifying COL1 deposition over time in combination with molecular data using #transcriptomics, #phosphoproteomics and #secretomics.
June 27, 2025 at 1:29 PM
MetRS*-based deep cell-selective tissue proteomics and secretomics in vivo www.sciencedirect.co...

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#proteomics #prot-paper
November 24, 2025 at 8:20 AM