Santiago Mille (@santimillef) 's Twitter Profile
Santiago Mille

@santimillef

Mexicano 🇲🇽 - Electrical Engineer - Bioengineering PhD @Stanford - systems and mammalian synthetic biology

ID: 1224153370144849921

linkhttp://santiagomille.dev calendar_today03-02-2020 02:11:30

155 Tweet

144 Followers

748 Following

Xiaojing Gao (@synbiogaolab) 's Twitter Profile Photo

Having often dealt with binder-limited projects, we sought a more accessible source for nanobodies than yeast display or llama. Here we introduce Germinal, computationally designing antibody-like binders with such a hit rate that only tens need to be screened for each target.

Having often dealt with binder-limited projects, we sought a more accessible source for nanobodies than yeast display or llama. Here we introduce Germinal, computationally designing antibody-like binders with such a hit rate that only tens need to be screened for each target.
Claudia Driscoll (@driscoll_cl) 's Twitter Profile Photo

Not only can we now build AI-generated bacteriophages... we can design de novo antibodies to bind them! With Germinal, a new pipeline for de novo antibody design, we move closer to a world where antibodies can be designed against virtually any protein, on demand. Check it out:

Talal Widatalla (@talaldotpdb) 's Twitter Profile Photo

Entering my PhD, de novo antibody design was a grand challenge I thought would not be solved without huge increases in affinity data and Ab-Ag structure. Only 2 years later, we provide the first open-source recipe to get antibody binders, almost magically, out of a computer (1/3)

AY 🌹 (@fascondo) 's Twitter Profile Photo

Designing, making, and testing antibodies the “old-fashioned way” kicked my ass back in the day. I think the next step here would be a similar pipeline for the manufacturing and testing. A lot of potential. 4-22% seems “low” until you experience what it entails.

Diego del Alamo (@ddelalamo) 's Twitter Profile Photo

Still boggles my mind that we can leave frameworks as-is and only edit CDRs and still reliably get nM binders. Complete opposite of what I would have expected given how hard it is to graft CDRs from one FW to another (such as humanizing mouse mAbs). First RFantibody and now this

Aditi Merchant (@aditimerch) 's Twitter Profile Photo

What if we could autocomplete DNA based on function? Today in nature, we share semantic design—a strategy for function-guided design with genomic language models that leverages genomic context to create de novo genes with desired functions.🧵 nature.com/articles/s4158…

Santiago Mille (@santimillef) 's Twitter Profile Photo

Go vote for Germinal designs! Both VHH and scFvs were designed. Click the STAR at the top-right. Here are some entries using our method: proteinbase.com/collections/ni… proteinbase.com/collections/ni… proteinbase.com/collections/ni… proteinbase.com/collections/ni… proteinbase.com/collections/ni…

Claudia Driscoll (@driscoll_cl) 's Twitter Profile Photo

may the prettiest binders win ⭐️ proteinbase.com/collections/ni… ⭐️ proteinbase.com/collections/ni… ⭐️ proteinbase.com/collections/ni… ⭐️ proteinbase.com/collections/ni… ⭐️ proteinbase.com/collections/ni…