Bernat Crosas (@CrosasLab) header
Bernat Crosas (@CrosasLab) profile picture

Biomedical researcher at the Institute of Molecular Biology of Barcelona. Our discoveries could help people

Joined February 2013
Well done, sister!
Thanks @CODATANews community! I look forward to working with all of you to help improve access and use of data for better science.
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Extraordinary mechanistic dissection of proteasome activities and definition of roles of ubiquitin beyond substrate recruitment. Always @AndyMartinLab ! pubmed.ncbi.nlm.nih.gov/3656…
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Bernat Crosas retweeted
Our paper describing the 3Å #cryoEM structure and chain-elongating function of UBR5, one of the largest HECT E3 ligases, is now out! at embopress.org/doi/full/10.15…
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If you're interested in degrading the "undruggable", you should pay close attention to what aptamers can do for you. #TPD pubmed.ncbi.nlm.nih.gov/3738…
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Join us next week for #DegradoZoom on July 6th, 12pm EST: Bernat Crosas @CrosasLab IBMB: Development of proteolytic chimeras based on direct 26S proteasome targeting Muhar Matthias @matthias_muhar ETH Zürich: A chemical degron marks C-terminally modified proteins for degradation
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Sala plena en el retorn de @CienciaAteneu! 📊 De què parlem quan parlem de dades? Realitats, Mites i Futurs Amb Pau Garcia, de @domesticstream i @mercecrosas, del @BSC_CNS
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July 6th, 12pm EST Bernat Crosas @CrosasLab (IBMB) 26S proteasome PROTACs. @matthias_muhar (ETH Zürich) C-terminal chemical degron.
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Bernat Crosas retweeted
Certain MEK inhibitors induce a complex between #MEK & difficult-to-degrade #cRAF. This allows bystander degradation of recalcitrant cRAF w/ #PROTACs targeting MEK. Excellent study by the Duncan & Jin labs @FoxChaseCancer @IcahnMountSinai @biorxivpreprint biorxiv.org/content/10.1101/…
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Fascinating parallel architecture and functioning of Npl4-Ufd1-CDC48 and 19S Proteasome complexes. The same evolutionary solution put together twice in the same pathway: Ubiquitin recognition, MPN domains and ATPase engine. #TPD pubmed.ncbi.nlm.nih.gov/3673… pubmed.ncbi.nlm.nih.gov/3731…
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Can allostery be decoded? the complexity of allosteric regulation, essential to understand cell biology and pharmacology, approached from different standpoints in two outstanding papers: elifesciences.org/articles/8… nature.com/articles/s41586-0…
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Let's be clear: this is beauty. (historical picture of Ordesa valley, #MontePerdido presiding, at the heart of Pirineo de Huesca)
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Spectacular tuning effect of Usp14 mediated by 3 allosteric checkpoints that make the 26S proteasome even more sophisticated. Thanks Y. Mao, D. Finley and all contributors. Retain in memory. nature.com/articles/s41586-0…
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The 26S proteasome is this fantastic machine that nature has created to achieve homeostatic control of intracellular protein content in a timely and perfectly regulated manner. Most of the strategies used in the #TPD field rely on that. #Proteindegradation
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If we have to have northern lights, let’s have northern lights.
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Bernat Crosas retweeted
nature.com/articles/s41467-0… In where we show that dynein adaptors, like most things in life, are also regulated by phosphorylation. Featuring: BICD2 and PLK1. You heard that right: no NEKs this time (but, of course, just wait).
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Bernat Crosas retweeted
Today we have received the Narcís #Monturiol medal from #conseller @quimnadal @recercauniscat This wouldn’t have been possible without an amazing Team 🔝🔝 and the continued support of @UABBarcelona @IBB_UAB @Biociencies_UAB Thanks ☺️
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I dont want to be part of a system that is so horrifically broken and serves to benefit the few 🧵5/5
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#Ubiquitin is really amazing. Virtually unchanged during eukaryotic evolution, it has generated thousands of functionally related genes, including hundreds of ubiquitin ligases, and is involved in almost all events related to #proteostasis. #Targetedproteindegradation (#TPD)
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