Matthias Trost

Matthias Trost

@mtrost.bsky.social

Professor of Proteomics. Currently at Newcastle University UK. he/him Here in personal capacity.

1.9K followers1.9K following165 posts

Matthias Trost reposted

So happy to have this work out and to continue applying our cutting-edge mass spectrometry approaches to study the clearance of apoptotic cells by #Macrophages.

Matthias Trost@mtrost.bsky.social

New paper from our lab. Driven by Ben Raymond, who now is a BBSRC fellow and builds his own line of research on this paper. Ben developed a method to define the proteome of macrophages after uptake of SILAC-labelled apoptotic cells. 1/2 www.nature.com/articles/s41...

New paper from our lab. Driven by Ben Raymond, who now is a BBSRC fellow and builds his own line of research on this paper. Ben developed a method to define the proteome of macrophages after uptake of SILAC-labelled apoptotic cells. 1/2 www.nature.com/articles/s41...

nature.comEfferocytosis triggered proteomic reprogramming of macrophages reveals CD97 as a novel apoptotic receptor - Cell Death & DifferentiationCell Death & Differentiation - Efferocytosis triggered proteomic reprogramming of macrophages reveals CD97 as a novel apoptotic receptor

Macrophages are reprogrammed after uptake of apoptotic cells and induce CD97 which he then shows is a apoptotic receptor. This is evolutionary conserved from fly, to mouse and human. 2/2

We have a 2-year postdoc position available for a bacterial infection biologist. We will use our exciting PhagoCyt method which uses flow cytometry to isolate pathogen-containing phagosomes & sensitive proteomics. Research Associate at The University of Manchester www.jobs.ac.uk/job/DSK144/r...

jobs.ac.ukResearch Associate at The University of ManchesterExplore an exciting academic career as a Research Associate. Don't miss out on other academic jobs. Click to apply and explore more opportunities.

If you need another reason to use proteomics to quantify proteins rather than Western Blot:

Reese Richardson@reeserichardson.bsky.social

The Thermo Fisher situation keeps getting worse. We've now collected 450+ problematic images presented as verification data in TF's antibody catalog. This includes: 🖌️ Dozens more images with duplications or painting 🖨️ Hundreds of blots that all share the same background (behold slideshow below)

I have a PhD position available with start date September 2026 at the University of Manchester. Proteomics analysis of flow cytometry-based isolated pathogen-containing phagosomes Due to funding requirements, this position is for UK home students only. www.findaphd.com/phds/project...

findaphd.comProteomics analysis of flow cytometry-based isolated pathogen-containing phagosomes at The University of Manchester on FindAPhD.comPhD Project - Proteomics analysis of flow cytometry-based isolated pathogen-containing phagosomes at The University of Manchester, listed on FindAPhD.com

Reposting this. If you are interested in applying for this fellowship in a research area of our lab's interest, let me know.

Michael Brockhurst@brockhurstlab.bsky.social

Three Bicentenary research fellowships on offer at @officialuom.bsky.social @fbmh-uom.bsky.social for exceptional ECRs with <3y postdoc experience 3yrs salary + £30k pa research expenses Do you have a great idea & want to join @mermanchester.bsky.social? www.bmh.manchester.ac.uk/research/sup...

- as standard for most of us, applying a 1.5-fold cut off (representing a 2-3x sigma) limits false discoveries. - there seem to be instrument and method dependent differences in how many points per peak are necessary for good quantitation.

Using various ratios of a two and three-proteome mix enabled us to do several controlled quantitative experiments (CQEs). They are in our experience essential to test novel DIA methods. We identified a few recommendations such as: 2/4

- be cautious with "atypical" proteomics expts where a large number of proteins change. - the most important factor for filtering proteins to get very good quantitation is the number of quantified peptides. - that being said, "single peptide wonders" are still surprisingly well quantified. 3/4

In life sciences there are two types of people in my experience: those that embrace and exploit omics and other large scale data technologies and those who work on one problem at the time. I had many collaborators from either side. 1/2

unfortunately, I feel that the people from the latter group are the ones that shoot down grants (and papers) because in their mind we only generate "lists". However, these lists are hugely important for communities and just because they don't appreciate them, doesn't mean they are not useful.

The financial crisis of the HE sector in the UK now leads to increased numbers of grant and fellowship applications, pushing down the success rates. Since also overheads increased, in some cases we will see success rates halved. There is a BBSRC fellowship which will have a success rate of 5%.

Matthias Trost reposted

Two days left for abstract submission and early bird registration for BSPR2025!

Ed Emmott@edemmott.bsky.social

Less than one week to go until the deadline for abstract submission and early bird registration for the British Society for Proteome Research @ukbspr.bsky.social annual conference 2025 in Liverpool! Deadline is Friday May 16! For more details see here: www.bspr.org/annual-meeti...

Labour dropping Net Zero will lead to Reform voters still voting Reform and Labour voters voting for the Greens. God, show some spine and do what is right.

Zoë Crowther@zoecrowther.bsky.social

Labour MPs are starting to get nervous about net zero, after a disappointing set of election results A minister cast doubt over Ed Miliband's political future An MP said net zero could "play out the same way as Brexit" Story by me & @matildamartin.bsky.social 👇

Sigh. Want to go to two conferences in France and ideally take the train to reduce my CO2 output. To get to Paris I can either spend £500 to take the train or fly for £88. This is so fucked up.