Veesler lab
@veeslerlab.bsky.social
990 followers 360 following 11 posts
Pathogen entry into cells, host immune responses & vaccine design: structural biology, protein design, virology & immunology @hhmi.bsky.social @uofwa.bsky.social
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veeslerlab.bsky.social
Congratulations Jason! This is awesome
Reposted by Veesler lab
martinpacesa.bsky.social
Exciting to see our protein binder design pipeline BindCraft published in its final form in @Nature ! This has been an amazing collaborative effort with Lennart, Christian, @sokrypton.org, Bruno and many other amazing lab members and collaborators.

www.nature.com/articles/s41...
Reposted by Veesler lab
henrietteautzen.bsky.social
I am excited to share our latest preprint presenting the structure of human NHE6, a key endosomal Na⁺/H⁺ exchanger involved in Christianson syndrome.

We bring together #cryo-EM, NMR, SAXS, lipidomics, and functional assays for an integrative analysis of NHE6 architecture, function, and regulation.
Reposted by Veesler lab
joostsnijder.bsky.social
We sequenced the anti-RSV-F antibody 131-2a by mass spec and determined its epitope by cryoEM. New insights in postfusion specific binding and antigenic site I. Now published in ACS Infectious Diseases @pubs.acs.org.
pubs.acs.org/doi/10.1021/...
@xdh.bsky.social @hangryhobbit.bsky.social
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sjorsscheres.bsky.social
Our entrance into protein design! Inverse folding steered by external sources of information, and for multiple conformations. By the amazing @kaiyi94.bsky.social and @kjamali.bsky.social!
Download our code and try it yourself. 🥳
kaiyi94.bsky.social
Excited to share our paper at #ICML: All-atom inverse protein folding through discrete flow matching with @kjamali.bsky.social and @sjorsscheres.bsky.social : openreview.net/forum?id=8tQdw…. If you are at ICML, let’s connect and talk generative models&protein design!
OpenReview
Promoting openness in scientific communication and the peer-review process
https://openreview.net/forum?id=8tQdw…
Reposted by Veesler lab
cryoempapers.bsky.social
Loss of FCoV-23 spike domain 0 enhances fusogenicity and entry kinetics pubmed.ncbi.nlm.nih.gov/40634609/ #cryoem
veeslerlab.bsky.social
Our paper describing how in-host evolution of a recently emerged, highly pathogenic coronavirus modulates entry into cells, membrane fusion and likely pathogenicity has now been published in its peer-reviewed form!

Led by Ale Tortorici!

@hhmi.org

www.nature.com/articles/s41...
Loss of FCoV-23 spike domain 0 enhances fusogenicity and entry kinetics - Nature
The molecular mechanisms of cell entry for the recently identified highly pathogenic feline coronavirus FCoV-23 are characterized in detail.
www.nature.com
Reposted by Veesler lab
prasad.bsky.social
Our effort to try to do something for [cystic fibrosis (CF)] started as a basic science enterprise. That was a hard slog back in the 1980s. Nobody would have supported except NIH. Now, 30 years after that discovery, young people with CF get to plan for retirement instead of an early funeral.
A lot of what NIH funds is basic science, which focuses on discoveries that might or might not result in practical applications. How can you describe the value of basic science to the public? To most people, it seems nebulous. It might take 30 years of research to pay off in a practical way.
Yes, it’s hard for people to understand the importance of basic science. I think the best way to deal with that is to talk about examples.
I’ll reflect on my experience with cystic fibrosis research. The effort to try to do something for that almost-uniformly fatal disease started as a basic science enterprise to try to discover the nature of the gene that is misspelled. That was a hard slog back in the 1980s. Nobody would have supported [research into it] except NIH.
That work by my University of Michigan lab, working with Lap-Chee Tsui at the Hospital for Sick Kids in Toronto, led to the discovery of the gene [and the mutation that causes the disease] in 1989. Then, a partnership of NIH-funded research, philanthropy from the Cystic Fibrosis Foundation, and investments by biotech and pharma led to a therapeutic breakthrough.

Now, 30 years after the gene discovery, young people with cystic fibrosis are planning for retirement instead of an early funeral.
Reposted by Veesler lab
harmitmalik.bsky.social
I have exhorted others to share positive news even in these uncertain times for US science.

I am really excited that @tamanash.bsky.social’s first paper on the remarkable evolutionary gymnastics of dual-host viruses (even in single codons) is now online.

Follow along here 🧪🧵
veeslerlab.bsky.social
Fantastic team effort involving Kaitlin Sprouse, Mary-Jane Navarro, Jack Brown, Lexi Walls, Jimin Lee, Albert Seo, Cameron Stewart, Ben Merz, Samantha Zepeda, along with @kinglabipd.bsky.social Baric lab @tylernstarr.bsky.social lab Moderna SK Bioscience & many others!
Reposted by Veesler lab
biorxivpreprint.bsky.social
Phylogeny-driven design of broadly protective sarbecovirus receptor-binding domain nanoparticle vaccines https://www.biorxiv.org/content/10.1101/2025.05.11.652904v1
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joostsnijder.bsky.social
Simultaneous polyclonal antibody sequencing and epitope mapping by cryoEM and mass spec: how far can we go? Check out the final version of our paper in eLife:
elifesciences.org/articles/101...
Reposted by Veesler lab
joostsnijder.bsky.social
Excited to be giving this webinar soon. Hope to see you then!
Reposted by Veesler lab
melodygcampbell.bsky.social
Congrats to Jeremy Hollis on receiving the Weintraub Award! A well-deserved recognition to a person who exemplifies (and resembles?) Hal.
A photo of Jeremy Hollis posing as Hal Weintraub using a tissue culture hood. A photo of Hal Weintraub using a tissue culture hood.
Reposted by Veesler lab
reichowlab.bsky.social
#NIHFundedDiscovery

How do cells avoid the "kiss of death"?

Gap junctions share life-saving signals—but under stress, they shut down to prevent spreading cytotoxic damage.

#CryoEM reveals the molecular switches behind this process!

www.biorxiv.org/content/10.1...

www.biorxiv.org/content/10.1...
Reposted by Veesler lab
brianhie.bsky.social
We trained a genomic language model on all observed evolution, which we are calling Evo 2.

The model achieves an unprecedented breadth in capabilities, enabling prediction and design tasks from molecular to genome scale and across all three domains of life.
veeslerlab.bsky.social
And with participation of Amin Addetia & Ale Tortorici