Alfredo Sciortino
@asciortino.bsky.social
460 followers 380 following 36 posts
Biophysicist / cytoskeleton in vitro 🏙 Paris @CytoMorphoLab
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asciortino.bsky.social
New preprint out 🔥🔥 on my postdoc work with @manuelthery.bsky.social and @lblanchoin.bsky.social about how we can create sustained dynamic steady states of actin network inside microscopic wells that contract "forever" without collapsing! A thread 🧵
www.biorxiv.org/content/10.1...
asciortino.bsky.social
Thanks to @agudocanalejo.bsky.social and @raovutukuri.bsky.social [amongst the first ones to observe large fluctuations in GUVs!] for today's News and Views about our recent paper on active vesicle deformations - and I agree with the conclusion, it's just a beginning..! doi.org/10.1038/s415...
Synthetic cells get into shape - Nature Physics
Shape changes in biological cells are driven by an active network of biopolymers. Now, similar deformations are observed in synthetic cell membranes.
www.nature.com
asciortino.bsky.social
Grande Gianni!
giannijacca.bsky.social
Check out my interview on TGR Leonardo—the Italian science news program—about the research that I'll be starting at the Università della Calabria (subtitles generated with AI). ☀️

🔬more about my research and the project:
www.giannijacucci.com
asciortino.bsky.social
The Schaeffer magnum opus is out. 🔥
ghinabadih.bsky.social
And it’s FINALLY OUT 🎉
The new work from Schaeffer, Théry and colleagues provides revolutionary insights into the processes underlying #centrosome positioning in adherent cells.
Check out the article @jcb.org to unlock the full story behind these new results: hubs.la/Q03hQjdn0!
@drs88.bsky.social
jcb.org
Unlike eggs & mitotic cells, in adherent interphasic cells the centrosome is NOT positioned by a balance of forces along #microtubules, but by cell shape organization around the #centrosome: rupress.org/jcb/article/...
@lblanchoin.bsky.social
@manuelthery.bsky.social
@gelinmatthieu.bsky.social
asciortino.bsky.social
As always with @lauraal.bsky.social , the pleasrue is all mine ☺️ - thanks @crpp-bordeaux.bsky.social for the nice hospitality
lauraal.bsky.social
It was a pleasrue to have @asciortino.bsky.social with us last week at @crpp-bordeaux.bsky.social
Thanks for showing us the beauty of soft interface driven out-of-equilibrium :) - and the best explanation on nematic defects ever!
baretjc.bsky.social
Today we have a seminar by Alfredo Scortino from the CytoMorpholab, invited by @lauraal.bsky.social

Minimal cytoskeleton for Syn Cell !

@crpp-bordeaux.bsky.social
Reposted by Alfredo Sciortino
ulrichschwarz.bsky.social
Registration has started for the conference "Emerging Trends in the Physics of the Cell" in memoriam of Erich Sackmann at TU Munich from October 15-18 2025 www.cpa.tum.de/cpa/conferen...
asciortino.bsky.social
Interesting read. Some problems are just weirder than you'd say.
clivethompson.bsky.social
So, the DOGE kids intend to rewrite the social-security administration's COBOL code-base!

and they want to do it ...

... in *a few months*

I did a huge dive into COBOL a few years ago (www.wealthsimple.com/en-ca/magazi...) ...

... so let me explain why DOGE is *way* over its skis here

1/9
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www.wealthsimple.com
Reposted by Alfredo Sciortino
clivethompson.bsky.social
So, the DOGE kids intend to rewrite the social-security administration's COBOL code-base!

and they want to do it ...

... in *a few months*

I did a huge dive into COBOL a few years ago (www.wealthsimple.com/en-ca/magazi...) ...

... so let me explain why DOGE is *way* over its skis here

1/9
browse by category
www.wealthsimple.com
asciortino.bsky.social
I am very happy to share that my work on active deformations of lipid vesicles is finally out in Nature Physics. A nicer thread+movies coming soon, in the meantime:
www.nature.com/articles/s41...

Thx to Andreas, Hammad, Dmitry, Gerhard @laynefrechette.bsky.social and everybody else who contributed!
Reposted by Alfredo Sciortino
isabellagraf.bsky.social
We are organizing a conference for young researchers at the intersection between physics & biology: www.embl.org/about/info/c... @embl.org @events.embl.org @intcha.bsky.social
Please consider applying/registering -- the deadline is already in one week!
asciortino.bsky.social
81% of Elon Musk thinks Elon Musk is a genius.
A tweet by Elon Musk.
asciortino.bsky.social
You know the pain 🥰 gracias
asciortino.bsky.social
So.. thanks for reading! I hope you liked it - and check out the preprint. Also thanks to @manuelthery.bsky.social and @lblanchoin.bsky.social , to Magali in particular, and to all coauthors (I think only @alexandra-colin.bsky.social is here..)! www.biorxiv.org/content/10.1...
www.biorxiv.org
asciortino.bsky.social
So yes: filaments transport in 3D allows to separate a contractile flux at the bottom of the well with an extensile flux pushing filaments back to the periphery through the network's 3D architecture.
Scheme of the transport process inside microwells.
asciortino.bsky.social
If the DSS is through filament transport in 3D then severing those bundles in the middle of the well should stop it. So we performed laser ablation and *zap* the bundles are gone and the DSS contracts and dies out.
asciortino.bsky.social
Well apparently yes! The network uses its 3D architecture to "suck" filaments at the center and "inject" them back at the periphery - again, we show this with tracking filaments in 3D. But it's barely visible in the data, so we developed a killer experiment ;-) go to the next block to see it..
asciortino.bsky.social
Well, if it is not nucleation and it is not transport in 2D, we might as well take a look at the network architecture in 3D! Using confocal we observe this weird tent-like structure - is it possible that filaments are transported through it?
asciortino.bsky.social
What we find is that transport on the wells surface is coherent with actomyosin sliding combined with some "gliding" due to motors sticking to the membrane. But the net flux is still contractile, so what is pushing filaments back to the periphery...???
Graph of actin filaments' speed.
asciortino.bsky.social
It's not actin turnover, the classical answer: this DSS works in the absence of actin nucleators or in the presence of phalloidin, i.e. with stabilized filaments. No depolymerization is present. So it has to be transport of the filaments. We combine a bunch of techniques to observe it, like speckle.
asciortino.bsky.social
... and we got this: continuous actin contraction for hours and hours without collapse to the center. We also show how the flow and the actin architecture are organized in space in a regular way.
The question is... what is sustaining this dynamic state? What "compensates" for this contractile flow?