Our paper with @sokrypton.org using AlphaFold2 to predict small-molecule binding sites in proteins is now out in Nature Methods! π§΅
rdcu.be/e7SnX
www.nature.com/articles/s41...
Our paper with @sokrypton.org using AlphaFold2 to predict small-molecule binding sites in proteins is now out in Nature Methods! π§΅
rdcu.be/e7SnX
www.nature.com/articles/s41...
Not sure if they have an international commercial team. But I know their antibodies are quite good somehow, maybe I could reach out to them if you need? You can PM me if necessary.
I can tell Huabio is a real company!π
Thanks! I see, then anti-NRXN3Ξ± is impossible to detect NRXN3Ξ², but anti-NRXN3Ξ² has a possibility to detect NRXN3Ξ±.
Great tools! For anti-NRXN3a/b antibodies, does they recognize each other? I saw the test data, and most likely a does not cross with NRXNa families, and b does not cross with NRXNb families. It would be great to know does anti-NRXN3a antibody detect NRXN3b and vice versa.
Saw a familiar face. Congratulations Rohith!
Check out our newest work! This is a story on how to get selectivity in binders - both isoform and site selectivity. Read the paper or enjoy this brief Skytorial of what we did!
www.biorxiv.org/content/10.1...
1/n
How cool it is!!
How do cells adapt morphology to function? In a π₯ preprint by @zjmaggiexu.bsky.social , with @dudinlab.bsky.social and @amyweeks.bsky.social , we identify a self-organizing single-cell morphology circuit that optimizes the feeding trap structure of the suctorian P. collini. π§΅ tinyurl.com/4k8nv926
A parts list of promoters and gRNA scaffolds for mammalian genome engineering and molecular recording - @jshendure.bsky.social @troymcdiarmid.bsky.social @uwgenome.bsky.social go.nature.com/49eTPCu
Fun to see this thread answer some questions I had, thank you.
Cool! This could have a lot of influence on sensors, pull down, signaling rewiring...π€
I seeπ thank you!
I would like to hear some suggestions on why you think we should not use it?
π Our new paper is out @natmethods.nature.com!
Kuffer & Marzilli engineered conditionally stable MS2 & PP7 coat proteins (dMCP & dPCP) that degrade unless bound to RNA, enabling ultraβlow-background, single-mRNA imaging in live cells.
π www.nature.com/articles/s41...
𧬠www.addgene.org/John_Ngo/
Thank you, looks very cool! Can I message you about the cell marker you are using here?
Very cool! What kind of cell types are used here, and what kind of microscope is used? How long does the imaging take?
PANCS-Binders (phage-assisted noncontinuous selection of protein binders) screens multiple high-diversity protein libraries against a panel of dozens of targets for high-throughput binder discovery. @chembiobryan.bsky.social @mstyles-chembiol.bsky.social
www.nature.com/articles/s41...
That was so cool!
Humanized Caffeine-Inducible Systems for Controlling Cellular Functions https://www.biorxiv.org/content/10.1101/2025.06.13.659463v1
That was coolπ
Cool, intresting findings, could be invented as tool for transcription control?
Very cool study!
I have a lot of recommendations if you are in Chinaπ
Genomes encode biological complexity, which is determined by combinations of DNA mutations across millions of bases
In new work @arcinstitute.org, we report the discovery and engineering of the first programmable DNA recombinases capable of megabase-scale human genome rearrangement
Congrats! Useful tools!
Far-red chemigenetic kinase biosensors enable multiplexed and super-resolved imaging of signaling networks - @michellefrei17.bsky.social @jinzhanglab.bsky.social go.nature.com/3GfqrzL
Smart idea! Bring phos-sensor to transcription activation?
Wow, I heard the report before. Congratulations!
Wow, congratulations!