Martin Pacesa (@martinpacesa) 's Twitter Profile
Martin Pacesa

@martinpacesa

Structural biologist working on 🖥️ protein design, AI, and #CRISPR-Cas gene editing ✂️🧬 Avid weirdness connoisseur 🎩

ID: 1069570401972441088

calendar_today03-12-2018 12:33:50

1,1K Tweet

3,3K Followers

981 Following

Erman KARASU (@karasuerman1) 's Twitter Profile Photo

Have you ever wondered why some cell lines are easy to edit with CRISPR-mediated gene editing, while others are more difficult? Our paper is now online and offers an interesting answer: nature.com/articles/s4158…

Julian Englert (@julian_englert) 's Twitter Profile Photo

Less than 5 days to go for our protein design competition at Adaptyv Bio! We just updated the competition page with a virtual leaderboard for the top 10 designs ranked according to iPAE. Will be updated daily till the submission deadline on Sunday Aug 18! Can you beat the

Less than 5 days to go for our protein design competition at <a href="/adaptyvbio/">Adaptyv Bio</a>! 

We just updated the competition page with a virtual leaderboard for the top 10 designs ranked according to iPAE. 

Will be updated daily till the submission deadline on Sunday Aug 18! Can you beat the
Brad Krajina (@bradkrajina) 's Twitter Profile Photo

Blender soft body simulations are great for animating squishy things like cells, but they break if you make cells divide. So I'm building my own cell growth soft body simulator from the ground up in blender geometry nodes. Hope to release this tool soon. #b3d

Julian Englert (@julian_englert) 's Twitter Profile Photo

More than 700 designs by 90 amazing protein designers were submitted to our protein design competition! Given this awesome turnout we've decided to increase the number of proteins to be tested in the lab to 200 in order to validate more designs Check out foundry.adaptyvbio.com/egfr_design_co…

More than 700 designs by 90 amazing protein designers were submitted to our protein design competition!

Given this awesome turnout we've decided to increase the number of proteins to be tested in the lab to 200 in order to validate more designs

Check out foundry.adaptyvbio.com/egfr_design_co…
Ryota IINO 飯野亮太 (@ryotaiino) 's Twitter Profile Photo

Very happy collaboration with Prof. Yan Yu group Yan Yu Group! We visualized rotation of V-ATPase using Janus nanoparticle and measured torque using the fluctuation theorem! Visualizing Single V-ATPase Rotation Using Janus Nanoparticles biorxiv.org/content/10.110…

Kelvin Lau always @klausenhauser on ☁️ 🪡 🐘 (@klausenhauser) 's Twitter Profile Photo

Lots of great suggestions! SmithLabUMBC mentioned sulfate. But then this was definitely not present in the buffer. But there was a sulfur containing chemical.. the DMSO solvent in which the ligand was dissolved in. Probably exchanged with the Chlorines..

Lots of great suggestions! <a href="/SmithLabUMBC/">SmithLabUMBC</a> mentioned sulfate. But then this was definitely not present in the buffer.  But there was a sulfur containing chemical.. the DMSO solvent in which the ligand was dissolved in. Probably exchanged with the Chlorines..
Liwei Chang (@liwei_chang_) 's Twitter Profile Photo

Did AlphaFold solve the protein folding problem? ...Not yet! AF2 predicts static structures, usually the native state by default. However, we found AF2 can generate structures aligning well with known folding intermediates. biorxiv.org/content/10.110… Alberto Perez UF Chemistry 1/n

Neuroskeptic 🇺🇦 (@neuro_skeptic) 's Twitter Profile Photo

We need a Gordon Ramsay's Kitchen Nightmares for science. Gordon going into struggling labs, revealing the horrors lurking in fridges and file drawers, calling a postdoc a donkey.

elevyLab (@elevylab) 's Twitter Profile Photo

Years ago, we discovered that missense mutations in homomeric proteins can induce their supramolecular assembly, as in the 📽️👇 - Question: how are such aberrant assemblies of *folded* proteins handled in a eukaryotic cell? The answer here: biorxiv.org/content/10.110… + 🧵 below

Martin Pacesa (@martinpacesa) 's Twitter Profile Photo

Wow, this is really unexpected! Designs were done together with Lennart Nickel in Bruno Correia lab. Our pipeline will be fully open source and preprint online hopefully next week 🙂

Adaptyv Bio (@adaptyvbio) 's Twitter Profile Photo

The Protein Design Competition results are in! 🧬 200 designs tested in our lab 🌍 90 protein designers from around the world 💎 5 novel binders found 🎯 2.5% hit rate (vs 0.01% on previous EGFR work) 1st place: Martin Pacesa & Lennart Nickel 2nd place: @khRRustamov

The Protein Design Competition results are in!  

🧬 200 designs tested in our lab  
🌍 90 protein designers from around the world  
💎 5 novel binders found  
🎯 2.5% hit rate (vs 0.01% on previous EGFR work)  

1st place: <a href="/MartinPacesa/">Martin Pacesa</a> &amp; Lennart Nickel 
2nd place: @khRRustamov
Adaptyv Bio (@adaptyvbio) 's Twitter Profile Photo

The top binder from the competition was EGFR_l138_s90285_mpnn2, designed by Martin Pacesa and Lennart Nickel. Martin and Lennart used a structural hallucination approach where an initial random sequence is continually optimized by backpropagation through the AlphaFold2 network

The top binder from the competition was EGFR_l138_s90285_mpnn2, designed by <a href="/MartinPacesa/">Martin Pacesa</a> and Lennart Nickel. 

Martin and Lennart used a structural hallucination approach where an initial random sequence is continually optimized by backpropagation through the AlphaFold2 network