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GAMA Miguel Angel

@miangoar.bsky.social
259 followers 187 following 137 posts

Biologist that navigate in the oceans of diversity through space-time Protein evolution, metagenomics, AI/ML/DL Website miangoaren.github.io

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Reposted by GAMA Miguel Angel
Milot Mirdita @milot.bsky.social · 16/09/2026
ColabFold 1.6.3 is out! 2.5x faster, pip-installable, ipSAE+pDockQ2 scores. Thanks Choonghwan Lee, Marielle Russo, Gyuri Kim 🐍pip install colabfold[alphafold] CF2 Sneak Peak with AF3/Boltz/Protenix/ESMFold2… 🐍pip install "colabfold[alphafold3]@git+https://github.com/sokrypton/ColabFold@af3-preview"
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Sergey Ovchinnikov @sokrypton.org · 17/09/2026
Introducing highly experimental localfold.org Building on @martinsteinegger.bsky.social af2 webgpu port, @milot.bsky.social optimizations & jax ports of af3-like models by @marielle.bsky.social, Choonghwan Lee, Julia Buhmann. WARNING: runs directly on your 💻, may drain 🪫 & eat data📱 & overheat 🔥💻
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Martin Steinegger 🇺🇦 @martinsteinegger.bsky.social · 13/09/2026
Fold Spacer lets you fly through protein structures (Weekend project #2). It’s my first game: I originally set out to build a racer with structures as the tracks, but was a little too crazy. So it became this instead. You can upload your own structures. 🌐 martin-steinegger.github.io/Fold-Spacer/
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Sergey Ovchinnikov @sokrypton.org · 14/09/2026
Finally a more intuitaive way to learn pLDDT/pAE? 😎 sokrypton.github.io/protein_figh... (Character idea from @hannes-stark.bsky.social & Alex Waldherr)
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Protein Structure Evolution (ProSE) Seminar @proteinstructure.bsky.social · 01/09/2026
Join us next Tuesday, 5PM CET for our first ProSE after the summer! Betül Kaçar @kacarlab.bsky.social will talk about the origin and early evolution of ancient proteins! 📜🧬 tinyurl.com/prose-seminar2
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Lada Isakova @ladaisa.bsky.social · 03/04/2026
Excited to share that my first paper is finally out in @pnas.org! We ask what limits the exploration of protein sequence space and find that shared ancestry and divergence time play a much larger role than selection or epistasis. www.pnas.org/doi/10.1073/...
pnas.org
Descent from a common ancestor restricts exploration of protein sequence space | PNAS
How functional protein sequences are distributed in sequence space is fundamentally important for evolutionary theory and protein design, particula...
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Philip Romero @philromero.bsky.social · 18/08/2026
What if AI could interact directly with biology? Congrats to Coban, who gave AI the ability to experiment and learn through feedback. Over 25 autonomous rounds, it uncovered the determinants of enzyme specificity. Give AI the ability to experiment, then get out of the way. doi.org/10.64898/202...
doi.org
Learning protein function through autonomous experimental interaction
Biological AI learns primarily from existing observations, but many questions cannot be answered from available data alone. Here we show that AI can instead acquire knowledge by acting directly on biological systems and learning from the consequences. We developed a closed-loop framework in which autonomous agents design protein variants, construct and characterize them in a robotic laboratory, learn from the resulting experimental feedback, and decide what experiments to perform next. We then allowed the system to operate continuously and without human intervention for approximately one month, during which multiple agents independently explored protein sequence space while learning from shared experimental experience. Applied to glycoside hydrolases, the agents discovered enzymes with substantially altered substrate specificity toward non-native sugars and progressively learned the structure of the underlying sequence-function landscape. The resulting experimental experience also revealed determinants of substrate specificity and protein expression that were not specified as learning objectives. These results demonstrate that AI can autonomously interact with biology over extended periods to acquire knowledge through experience, establishing a framework for biological discovery driven by continuous experimental interaction. ### Competing Interest Statement The authors have declared no competing interest. National Institute of General Medical Sciences, 5R01GM150929
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Adam Phillippy @aphillippy.bsky.social · 06/08/2026
For the past 30 years, “whole-genome sequencing” has been a misnomer. Today the T2T Consortium publishes a dozen papers heralding a future of truly complete genomes for humans and nearly any vertebrate 👨‍🔬🐒🐦🐀🦒🐎🫏🐹🐟 (sorry, no salamanders): www.cell.com/consortium/t... 🧵[1/15]
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Martin Steinegger 🇺🇦 @martinsteinegger.bsky.social · 01/08/2026
Riboseek is a fast RNA/DNA search. More sensitive than nhmmer at 250x speed. Structure-aware realignment produces MSAs approaching rMSA quality. Plus 1.7M precomputed RNA MSAs, and an API to search your own 📄 www.biorxiv.org/content/10.6... 💾 github.com/steineggerla... 🌐 search.foldseek.com/riboseek
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Johanna von Wachsmann @johannavw.bsky.social · 16/06/2026
🧬 New preprint! We clustered 5.6 million bacterial genomes into genomically cohesive units (GCUs) 500× faster than existing tools. (In just 14 hours, 16.5 GB RAM using 48 CPUs). 🦠🐙Meet gemsparcl 💎✨! www.biorxiv.org/content/10.6...
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Martin Steinegger 🇺🇦 @martinsteinegger.bsky.social · 06/06/2026
Meet the Folddisco Marv, designed by Hyunbin Kim, who also developed Folddisco.
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Martin Steinegger 🇺🇦 @martinsteinegger.bsky.social · 06/06/2026
Folddisco is now published @natbiotech.nature.com. It’s a fast motif search for similar 3D DISCOntinuous residues like catalytic sites or zinc fingers across the entire protein universe. 📄 www.nature.com/articles/s41... 💾 folddisco.foldseek.com​​​​​​​​​​​​​​​​ 🌐 search.foldseek.com/folddisco
nature.com
Structural motif search across the protein universe with Folddisco - Nature Biotechnology
Folddisco enables protein structural motif search in million scale databases.
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GAMA Miguel Angel @miangoar.bsky.social · 20/05/2026
Today, the AlphaFold2 paper reached the milestone of 50k citations according to Google Scholar! And AlphaFold3 will likely reach 15k citations tomorrow. Congratulations to the entire AlphaFold team, as well as to all the scientists who helped democratize protein structure prediction 🥳
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Protein Structure Evolution (ProSE) Seminar @proteinstructure.bsky.social · 05/05/2026
Join ProSe next week Tuesday, when Noelia Ferruz @noeliaferruz.bsky.social is talking about "Controllable Protein Design with Protein Language Models and Reinforcment Learning", TUE, May 12, 5PM CET! Sign-up here: tinyurl.com/prose-seminar2
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ace-gtdb.bsky.social @ace-gtdb.bsky.social · 15/04/2026
GTDB release 11 based on RefSeq 232 (R11-RS232) is live at gtdb.ecogenomic.org. This release covers 901,341 genomes (23% increase) and has 199,923 species clusters (39% increase). Release notes at: forum.gtdb.ecogenomic.org/t/announcing.... Release statistics at: gtdb.ecogenomic.org/stats/r232.
gtdb.ecogenomic.org
GTDB - Genome Taxonomy Database
The Genome Taxonomy Database (GTDB) is an initiative to establish a standardised microbial taxonomy based on genome phylogeny.
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GAMA Miguel Angel @miangoar.bsky.social · 20/04/2026
1/12 🧵 Do you want to learn how to design proteins using AI but don’t know anything about biology? I created a free 10-lesson course on YouTube. It’s now available in Spanish (original) and English (autodubbing w/Kokoro 82M). Here’s an overview of the topics covered in each lecture :)
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Martin Steinegger 🇺🇦 @martinsteinegger.bsky.social · 17/03/2026
AlphaFold database has entered the era of complexes. Together with NVIDIA, DeepMind and EBI, we use ColabFold, OpenFold and MMseqs2-GPU to predict ~31 million complexes (homo & hetro-dimers) resulting in 1.8 million high-quality predictions 📄 research.nvidia.com/labs/dbr/ass... 🌐 alphafold.ebi.ac.uk
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Yun S. Song @yun-s-song.bsky.social · 21/02/2026
Can we simulate realistic evolutionary trajectories and “replay the tape of life”? In this work, we propose a flexible, generalizable deep learning framework for modeling how the entire protein sequence evolves over time while capturing complex interactions across sites. 1/n doi.org/10.64898/202...
doi.org
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Richard McElreath 🐈‍⬛ @rmcelreath.bsky.social · 12/02/2026
mel gibson passion of christ meme. Gibson looking comfortable, labeled HUMAN GENETICIST. Actor in bloody christ garb labeled PLANT GENETICIST
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GAMA Miguel Angel @miangoar.bsky.social · 12/02/2026
I am in the "Life Sciences Super Cluster" and quite far away from many colleagues in protein design who are in the cluster called "Computational Chemistry Nexus" 😭
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GAMA Miguel Angel @miangoar.bsky.social · 06/02/2026
Does anyone know the meaning of AlphaGenome and its impact? It’s not my area, so I don’t know how important it is. But I think is not equivalent to AlphaFold2, since no other area in biology has the high-quality data and structure provided by PDB, UniProt and CASP competition.
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GAMA Miguel Angel @miangoar.bsky.social · 06/02/2026
Sometimes I see Nature papers as elegant $13k commercials from AI companies inviting you to subscribe to their chatbots
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Reposted by GAMA Miguel Angel
Claudèle Lemay-St-Denis @claudele.bsky.social · 08/10/2025
How does catalysis emerge from non-catalytic domains? In our new paper, we show that catalytic activity can arise without conserved active-site residues — through multimerization and electrostatic features instead. A striking case of catalysis evolving from binding.
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Klara Hlouchova lab @hlouchova-lab.bsky.social · 03/11/2025
Can proteins fold and function with half of the amino acid alphabet? Using only 10 residues, we designed stable, mutation-resilient structures—no aromatics or basics involved. A minimalist foundation for ancient biology and synthetic design. tinyurl.com/37t8br4v #ProteinDesign #OriginsOfLife
tinyurl.com
Ancient amino acid sets enable stable protein folds
Early proteins likely arose from a chemically limited set of amino acids available through prebiotic chemistry, raising a central question in molecular evolution: could such primitive compositions yie...
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GAMA Miguel Angel @miangoar.bsky.social · 04/02/2026
I recorded ~4h where we cover the main bio databases, data processing methods, many sources of bias and topics like generalization and data leakage :) youtu.be/SKpHaHgvCKE Slides drive.google.com/file/d/1jpEwDBncJCRviG_DaWs2EpzCL_1BfB9t/view English is available only via auto-translated subtitles
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GAMA Miguel Angel @miangoar.bsky.social · 03/02/2026
I recorded ~8h introducing the main algorithms for protein design: from classical approaches to protein language models, AlphaFold, ESMFold, MPNN, diffusion models and more :) youtu.be/wKUYtAt87d4T... Slides drive.google.com/file/d/1EPLj... English is available only via auto-translated subtitles
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GAMA Miguel Angel @miangoar.bsky.social · 02/02/2026
I’ve recorded ~8h explaining the architectures of AlphaFold, AF2 & AF3, as well as the context needed to understand their development, applications and limitations :) youtu.be/_jDRr5BcTaY Slides drive.google.com/file/d/1i4QE... English is available only via auto-translated subtitles
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GAMA Miguel Angel @miangoar.bsky.social · 01/02/2026
The 7th lecture is available on YouTube :) We will review how proteins emerge and diversify throughout evolution, considering mutations and molecular interactions youtu.be/qaypRS8SX5M Slides drive.google.com/file/d/1BfQd... English is available only via auto-translated subtitles
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Kaçar Lab at UW-Madison @kacarlab.bsky.social · 30/01/2026
Our new paper, out today! We resurrected ancient nitrogenases first used by life on Earth 3 billion years ago. We combined synthetic biology and geology & validated their chemical #biosignature in rocks that helps reveal ancient life on Earth!(and beyond!) Link: www.nature.com/articles/s41...
nature.com
Resurrected nitrogenases recapitulate canonical N-isotope biosignatures over two billion years - Nature Communications
The study shows that nitrogenase enzymes have maintained stable isotope signatures over billions of years, revealing how ancient microbes shaped Earth’s nitrogen cycle and offering a new experimental ...
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Clockwork @watchclockwork.com · 31/01/2026
💪 NEW VIDEO: Flying over the A-band of an atomic-scale model of a vertebrate muscle sarcomere. Let's explore the molecular mechanics that make your muscles work. Rendered using @bradyajohnston.bsky.social 's molecular nodes Model based on the incredible work of the @raunser-lab.bsky.social lab
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GAMA Miguel Angel @miangoar.bsky.social · 31/01/2026
The 6th lecture is now available on YouTube :) We’ll review how proteins adopt their 3D shape, how they perform their functions and how their activity is regulated youtu.be/cZs8XtVYa5A Slides drive.google.com/file/d/1TpPj... English is available only via auto-translated subtitles
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GAMA Miguel Angel @miangoar.bsky.social · 30/01/2026
The fifth lecture of the course is now available on YouTube :) We’ll review amino acid chemistry and how we organize and classify proteins youtu.be/gE6qXwpBP_s Slides drive.google.com/file/d/1F99V... For now, the English version is only available through the automatic translation of the subtitles
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GAMA Miguel Angel @miangoar.bsky.social · 29/01/2026
The fourth lecture of the course is now available on YouTube :) We will review how Transformers and modern LLMs work youtu.be/vUpb6O6T2yQ Slides drive.google.com/file/d/1y2Vj... For now, the English version is only available through the automatic translation of the subtitles.
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GAMA Miguel Angel @miangoar.bsky.social · 28/01/2026
The third lecture of the course is now available on YouTube :) We will review how neural networks work. youtu.be/pAgL7NsCUMU Slides drive.google.com/file/d/1cazt... For now, the English version is only available through the automatic translation of the subtitles.
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GAMA Miguel Angel @miangoar.bsky.social · 27/01/2026
The second lecture of the course is now available on YouTube :) We will review what AI is, its subfields and how to train a model. youtu.be/Xx80O85-5rI Slides drive.google.com/file/d/1i-Jo... For now, the English version is only available through the automatic translation of the subtitles.
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GAMA Miguel Angel @miangoar.bsky.social · 27/01/2026
The first lecture of the course is now available on YouTube :) youtu.be/uMkZzKbnoJI Slides drive.google.com/file/d/1uDwe... For now, the English version is only available through the automatic translation of the subtitles.
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GAMA Miguel Angel @miangoar.bsky.social · 22/01/2026
🧵1/3 I created this free 37-hour course, distributed across 10 lectures, to introduce AI-based protein design. For more information about the course and its specific topics, please visit the official course page:
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Prof Jenny Rohn @jennyrohn.bsky.social · 21/01/2026
Cost of being female lead/corresponding author in biomedical sciences: "[T]he median amount of time spent under review is 7.4%–14.6% longer for female-authored articles than for male-authored articles" even in disciplines where women well-represented. #AcademicSky journals.plos.org/plosbiology/...
journals.plos.org
Biomedical and life science articles by female researchers spend longer under review
Women are underrepresented in academia, especially in STEMM fields, at top institutions, and in senior positions. This study analyzes millions of biomedical and life science articles, revealing that f...
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Milot Mirdita @milot.bsky.social · 20/01/2026
My time in @martinsteinegger.bsky.social's group is ending, but I’m staying in Korea to build a lab at Sungkyunkwan University School of Medicine. If you or someone you know is interested in molecular machine learning and open-source bioinformatics, please reach out. I am hiring! mirdita.org
mirdita.org
Mirdita Lab - Laboratory for Computational Biology & Molecular Machine Learning
Mirdita Lab builds scalable bioinformatics methods.
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Colin Jackson @cjjackson.bsky.social · 20/01/2026
www.biorxiv.org/content/10.6... most proteins are multi domain but our understanding of how architectures evolve is limited - we mapped 40K chitinases and show a stepwise “grammar” of domain gain/loss and localisation changes that predicts ecological strategy and physiological function.
biorxiv.org
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GAMA Miguel Angel @miangoar.bsky.social · 09/10/2025
I just want to create hype and say that I made a 10-class course to introduce people to AI-driven protein design. It’s around 750 slides and will be freely available for anyone who wants to use them and, most importantly, improve them. Stay tuned :)
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GAMA Miguel Angel @miangoar.bsky.social · 16/01/2026
1/2 If you think that the Protein Data Bank is a representative DB, it is not. The data is highly biased. The CATH suggests that there are 1,472 protein folds, yet among the ~600k domains present in the PDB, ~39% are represented by the 10 most abundant folds (AKA superfolds).
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Claudia Alvarez Carreño @claudiaalcar.bsky.social · 09/01/2026
Thrilled to introduce TEDLH, a library of profile HMMs built from TED’s structure-derived domain annotations of the AFDB. Explore 765K HMMs capturing CATH superfamily diversity. www.biorxiv.org/content/10.6...
Construction of TEDLH from TED domain annotations.
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Albert Heck @hecklab.bsky.social · 04/09/2025
🕷️Spiders in your blood? Don’t worry, these are protein molecules of C4BP protein, part of your immune system. Just like real spiders, they grab prey with their “legs.” Watch them in action! Intrigued, check the paper of @tkadava.bsky.social doi.org/10.1016/j.mc... @bijvoet-centre.bsky.social
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Brett Baker @archaeal.bsky.social · 26/11/2025
youtu.be/Jy_boPdY0zo?...
youtu.be
The Origins of Complex Life | Searching for the Asgards
YouTube video by Schmidt Ocean
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Dawid Zyla @dzyla.bsky.social · 23/11/2025
Proteins are dynamic structures, but structural biology often shows them as static snapshots. Inspired by long-exposure photography and generative art, I built ProteinCHAOS, an artistic tool inspired by molecular dynamics to capture protein flexibility over time, much like long-exposure images.
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Mark A. Hanson @hansonmark.bsky.social · 11/11/2025
We wrote the Strain on scientific publishing to highlight the problems of time & trust. With a fantastic group of co-authors, we present The Drain of Scientific Publishing: a 🧵 1/n Drain: arxiv.org/abs/2511.04820 Strain: direct.mit.edu/qss/article/... Oligopoly: direct.mit.edu/qss/article/...
A table showing profit margins of major publishers. A snippet of text related to this table is below.

1. The four-fold drain
1.1 Money
Currently, academic publishing is dominated by profit-oriented, multinational companies for
whom scientific knowledge is a commodity to be sold back to the academic community who
created it. The dominant four are Elsevier, Springer Nature, Wiley and Taylor & Francis,
which collectively generated over US$7.1 billion in revenue from journal publishing in 2024
alone, and over US$12 billion in profits between 2019 and 2024 (Table 1A). Their profit
margins have always been over 30% in the last five years, and for the largest publisher
(Elsevier) always over 37%.
Against many comparators, across many sectors, scientific publishing is one of the most
consistently profitable industries (Table S1). These financial arrangements make a substantial
difference to science budgets. In 2024, 46% of Elsevier revenues and 53% of Taylor &
Francis revenues were generated in North America, meaning that North American
researchers were charged over US$2.27 billion by just two for-profit publishers. The
Canadian research councils and the US National Science Foundation were allocated US$9.3
billion in that year.A figure detailing the drain on researcher time.

1. The four-fold drain

1.2 Time
The number of papers published each year is growing faster than the scientific workforce,
with the number of papers per researcher almost doubling between 1996 and 2022 (Figure
1A). This reflects the fact that publishers’ commercial desire to publish (sell) more material
has aligned well with the competitive prestige culture in which publications help secure jobs,
grants, promotions, and awards. To the extent that this growth is driven by a pressure for
profit, rather than scholarly imperatives, it distorts the way researchers spend their time.
The publishing system depends on unpaid reviewer labour, estimated to be over 130 million
unpaid hours annually in 2020 alone (9). Researchers have complained about the demands of
peer-review for decades, but the scale of the problem is now worse, with editors reporting
widespread difficulties recruiting reviewers. The growth in publications involves not only the
authors’ time, but that of academic editors and reviewers who are dealing with so many
review demands.
Even more seriously, the imperative to produce ever more articles reshapes the nature of
scientific inquiry. Evidence across multiple fields shows that more papers result in
‘ossification’, not new ideas (10). It may seem paradoxical that more papers can slow
progress until one considers how it affects researchers’ time. While rewards remain tied to
volume, prestige, and impact of publications, researchers will be nudged away from riskier,
local, interdisciplinary, and long-term work. The result is a treadmill of constant activity with
limited progress whereas core scholarly practices – such as reading, reflecting and engaging
with others’ contributions – is de-prioritized. What looks like productivity often masks
intellectual exhaustion built on a demoralizing, narrowing scientific vision.A table of profit margins across industries. The section of text related to this table is below:

1. The four-fold drain
1.1 Money
Currently, academic publishing is dominated by profit-oriented, multinational companies for
whom scientific knowledge is a commodity to be sold back to the academic community who
created it. The dominant four are Elsevier, Springer Nature, Wiley and Taylor & Francis,
which collectively generated over US$7.1 billion in revenue from journal publishing in 2024
alone, and over US$12 billion in profits between 2019 and 2024 (Table 1A). Their profit
margins have always been over 30% in the last five years, and for the largest publisher
(Elsevier) always over 37%.
Against many comparators, across many sectors, scientific publishing is one of the most
consistently profitable industries (Table S1). These financial arrangements make a substantial
difference to science budgets. In 2024, 46% of Elsevier revenues and 53% of Taylor &
Francis revenues were generated in North America, meaning that North American
researchers were charged over US$2.27 billion by just two for-profit publishers. The
Canadian research councils and the US National Science Foundation were allocated US$9.3
billion in that year.The costs of inaction are plain: wasted public funds, lost researcher time, compromised
scientific integrity and eroded public trust. Today, the system rewards commercial publishers
first, and science second. Without bold action from the funders we risk continuing to pour
resources into a system that prioritizes profit over the advancement of scientific knowledge.
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GAMA Miguel Angel @miangoar.bsky.social · 24/10/2025
I strongly recommend making cat-based diagrams to illustrate complex topics in protein science: "Figure 4 considers [...] invariance and equivariance with respect to translations and rotations in 3D. For illustration purposes, the figure includes a series of cat cartoons in 2D."
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GAMA Miguel Angel @miangoar.bsky.social · 09/10/2025
I just want to create hype and say that I made a 10-class course to introduce people to AI-driven protein design. It’s around 750 slides and will be freely available for anyone who wants to use them and, most importantly, improve them. Stay tuned :)
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Claudia Alvarez Carreño @claudiaalcar.bsky.social · 15/09/2025
Happy to share Piecing Together the History of Protein Folds From a Fragmented Evolutionary Record 🧪 It appears as part of a Special Section in @genomebiolevol.bsky.social organized by @cpuentelelievre.bsky.social @proteinmechanic.bsky.social and J. Douglas doi.org/10.1093/gbe/...
doi.org
Piecing Together the History of Protein Folds From a Fragmented Evolutionary Record
Abstract. Protein folds are structural units defined by the number, type, arrangement, and orientation of their core secondary structural elements. The uni
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