The de Botton Institute for Protein Profiling provides cutting-edge, comprehensive, and quantitative analysis of proteins in biological samples using mass spec.
Proteomics people, I need help troubleshooting a set of single cell runs. This is a SCOPEMS experiment, FACS sorting into 384 plate, digestion in the plate, TMT10, carrier of 100cells, controls and 6 single cells per TMT batch. I ran them on the Exploris 480+FAIMS (-45,-65)
Adding to the body of data for booster shot effectiveness, a new @TheLancet report of over 728,000 people w/ 3 shots vs >728,000 matched controls (2 shots):
93% reduction of Covid hospitalizations
https://t.co/cVpANpnkHs
Excited to share the next @YMerbl project where we used #CellularDumpsterDiving to find a new proteasome regulator of immunotherapy responses in lung cancer. Check out the @biorxivpreprint https://t.co/yJPuuchaDS and short thread 👇 (1/5)
Just completed protein extraction and total conc. measurement from 396 human brain samples. Going for glycoproteomic profiling in collaboration with Dr. Michal Beeri.
We are happy to share our joint paper with Dr. Shilo Rosenwasser, HUJI. Together, we developed a proteomics approach for global quantification of the thiol-proteome. https://t.co/AFaUnvvxzA
Proteomics folks out there, I have a question about correction for multiple hypothesis testing (FDR). We find a lot of experiments when Q vales are very high with p values very low. We validate the results and find they are indeed significant. What would you do in such cases?
We completed yet another basic course in mass spectrometry based proteomics. It��s so rewarding to see people who know very little about about this technology, complete the course with the ability to explain, in a presentation, the process of identifying and quantifying proteins.
Our SPEAR method is online, waiting on pear reviews. A new redox-proteomics approach based on differential labeling of oxidized and reduced cysteines with light and heavy isotopic forms of commercially available isotopically-labeled N-ethylmaleimide (NEM). No need for enrichment
Occasionally we get samples with polymers. It turns out with FAIMS, we can gas-phase separate/filter them out. Pretty cool!! (lower is -45, upper is -65)