Samson Petrosyan retweeted
After six years in stealth, Atomic Machines is out. Our mission: on-demand, universal command of matter. First beachhead: the Matter Compiler, an AI-native manufacturing system that builds working micro-machines from code alone. No per-product tooling. No process development. Different code, different machine.
We announced an agreement to acquire a nationwide low-band spectrum license portfolio that will pave the way for @Starlink to become a major mobile carrier in the US.
With this new spectrum and our Gen2 constellation, Starlink Mobile can ensure Americans have access to high-speed mobile broadband no matter where they are → spacex.com/updates#starlink-…
Samson Petrosyan retweeted
Today we announced the Claude-led discovery of a molecular machine that we suspect could represent a new gene editing mechanism. Its precise function, biotechnological utility (if any), or level of significance is not yet clear, but at minimum it is work I would have been proud to do as a PhD student. The work was done mostly, though not entirely, by Claude: our life sciences team suggested a broad area of research, Claude read through the literature and a bunch of genome data and discovered something interesting, then Claude proposed experiments to verify the discovery and our team carried them out.
It’s easy to dismiss this as a one-off or curiosity, but we’ve repeatedly seen a pattern where AI performance in new intellectual domains goes from weak to superhuman in a matter of a few years. In 2023 models struggled to do math at the level of an average high-school student. In 2024 they started to do well on math competitions for the best high-schoolers in the country, in 2025 they started to solve minor open problems, in early 2026 more significant open problems, and in late 2026 they are beginning to solve the top few open problems in all of mathematics. We believe AI for biology is on a similar exponential trend.
The main difference between biology and mathematics, of course, is that math can be done purely theoretically, while biology requires experimentation. Some have used this to draw the conclusion that AI’s utility in biology will be limited. We think this is wrong. As we’ve demonstrated today, humans can collaborate with AI to perform the experiments, validate key results in a few weeks and, if necessary, work with the AI to iterate on what they find. Eventually it may even be possible for Claude itself to safely perform the experiments by autonomously controlling lab equipment, with appropriate safeguards in place, but we aren’t doing that today (our lab is also a BSL1/BSL2 facility that doesn't handle materials dangerous to humans).
More broadly, biomedical advancement has many stages — from fundamental biology discoveries, to translational research, to drug discovery, clinical trials, and finally the actual delivery of medicines and health care to patients. We are also interested in these later stages, but even simply accelerating the first stage of fundamental biological discoveries has the potential to speed up and broaden the entire pipeline. Improving our understanding of biology and sharpening biologists’ tools can drive forward all of the later stages, for example by identifying new drug targets, finding new therapeutic modalities, allowing for more precise measurement, and speeding up the experimental loop which itself further accelerates our understanding of biology. This will not in itself speed up clinical trial times, but if it succeeds it could greatly increase the number of promising candidates that go into the pipeline — an increase in throughput even though latency remains.
In Machines of Loving Grace, I wrote about AI’s potential to “cure most diseases in 5-10 years” — a goal that sounds impossible, but one I believe is just barely possible if AI is applied to every stage of the pipeline. The first step is showing that AI can first help with, and then drive, biological discoveries.
Claude’s discovery is the latest in a line of related prior work that goes back decades, beginning with systems like CRISPR, and continuing with discoveries like the bridge recombinase and VIPR in the past few years. Recently, there has been heightened interest in systems based on reverse transcriptase (RT) enzymes, the enzyme underlying the system Claude identified. And most recently, a Stanford team working independently described a novel RT system with an associated non-coding array that is in some ways similar to the one Claude found, though they are distinct systems that evolved independently from each other. I believe that we’re at the very beginning of finding such systems and developing them into powerful tools for biotechnology.
I’m proud of the resources Anthropic has invested in accelerating the public benefits of AI through the life sciences, and we’re aiming both to grow our life sciences team and to work with other scientists to extend this approach to a broad range of problems. If you have a proposal for a research collaboration or are interested in joining our life sciences team, please reach out.
Claude has discovered a previously unknown enzyme system hidden in the DNA of bacteriophages. Beside the enzyme’s gene sits a long array of repeating DNA—a structure that looks somewhat similar to CRISPR.
We don’t yet understand what this system does, but only a handful of known systems share its features, and all of them are able to cut, copy, and paste DNA. Historically, the discovery of such programmable systems has helped revolutionize medicine. CRISPR, for instance, is now the foundation of genetic medicines. But it will take much more work to learn what this system does, and whether it can be put to similar use.
Read more: anthropic.com/news/claude-di…
Samson Petrosyan retweeted
Happy to share that I was named one of TIME’s 2026 Longevity Leaders. Our work uses physics-style theory to look for simple principles that can explain the complex dynamics of aging.
time.com/collection/longevit…
Samson Petrosyan retweeted
In case you missed the news, a new @OpenComputePrj (OCP) workstream has launched to create a shared reference architecture for the industry’s interconnect transition to silicon photonics. This effort brings together industry leaders to build a unified blueprint that mitigates ecosystem fragmentation, facilitates interoperability, and aligns with hyperscaler build flows. Watch Founder and CEO Nick Harris discuss how this standards initiative helps build the photonic foundation for next-gen AI infrastructure. @theanalognick @ConvergeDigest @NextGenInfra_io @WireRoy @AvidThink
Samson Petrosyan retweeted
This is a big deal. We're working with our 19 world-class industry partners to define the future of AI data centers with photonics.
We're moving towards creating the gold-standard for what photonics-enabled racks will look like
#cpo #npo #photonicinterposer #lightmatter
19 industry leaders and innovators. A blueprint for the photonic future of AI.
A new @OpenComputePrj (OCP) workstream has been launched to build a shared reference architecture for photonic interconnects, turning CPO from concept into hyperscale reality. The blueprint is laid out in the whitepaper, “Architecture Vision: Open Silicon Photonics for AI Systems.”
Lightmatter is proud to have played a lead role in organizing this coalition and grateful to every member for the expertise and commitment they've brought to this work. Read more: lightmatter.co/press-release…
Samson Petrosyan retweeted
Not just “someone”, but @Berkeley_EECS alum Nicholas Carlini.
someone at ANTHROPIC just showed CLAUDE finding ZERO DAY vulnerabilities in a live conference demo
claude has found zero day in Ghost, 50,000 stars on github, never had a critical security vulnerability in its entire, history...
it found the blind SQL injection in 90 minutes, stole the admin api key, then did the exact, same thing to the linux kernel
Samson Petrosyan retweeted
I’d cancel your AG1 subscription. They just completed a clinical trial and the results show no clinical benefit.Â
This has been obvious for years. AG1 has no real product substance and is fundamentally an influencer heist. Â
Two simple alternatives (75% and 56% less $), outperform AG1 in randomized clinical trials.
Two simple mono-ingredient alternatives that outperform AG1:
1. Chicory inulin 12 g daily ($20/mo)
2. Resistant starch 30 g daily for 12 weeks ($35/mo)
AG1 is not worth $79/mo.
AG1 study results (4-weeks, N=30):
+ No significant changes in blood biomarkers compared to placebo (CBC, CMP, lipids).
+ No statistically significant improvement in digestive quality-of-life scores (p = 0.058).
+ No significant metabolic or inflammatory biomarker benefits of any kind within the scope of what was measured in the trial.
+ Only small shifts in microbiome taxa but clinically irrelevant at this stage.
+ The intervention did not increase microbiome diversity compared to placebo. Alpha diversity was unchanged, and the taxa changes seen were only from pre- to post-analysis within each group. Between-group differences were limited, and the placebo actually showed similar or even potentially larger shifts. This means the observed changes fall within normal placebo-driven variability, not a real treatment effect. No global microbiota shifts were detected.
Chicory inulin 12 g in constipation patients
+ 12 g of chicory inulin daily for 4 weeks (compared to maltodextrin placebo)
+ Global microbiota shifts: enrichment in butyrate-producing Bifidobacterium and Anaerostipes, and depletion of the pro-inflammatory Bilophila.
+The effect was seen by comparing intervention vs placebo in a cross-over setting, a very rigorous type of clinical analysis in which each person serves as their own control, eliminating a lot of individual random noise.
+ The trial also met its primary objective by improving constipation symptoms in the targeted patient group.
Resistant starch daily 30g for 12 weeks in older adults
+ Significant increase in Bifidobacterium in both middle-aged and elderly participants, with an increase in the beneficial microbiome byproduct butyrate, and reductions in Proteobacteria (including inflammatory Escherichia–Shigella) in the elderly.
+ Resistant starch also significantly reduced blood glucose, and produced greater reductions in blood insulin and insulin resistance (HOMA-IR) in the elderly group.
Samson Petrosyan retweeted
Replying to @william_fitz
$60bn each is not “a little bit of extra”
Larry and Sergey can’t stay in California since the wealth tax as written would confiscate 50% of their Alphabet shares.
Each own ~3% of Alphabet's stock, worth about $120 billion each at today's ~$4 trillion market cap.
But because their shares have 10x voting power, the SEIU-UHW California billionaire tax would treat them as owning 30% of Alphabet (3% Ă— 10 = 30%). That means each founder's taxable wealth would be $1.2 trillion.
A 5% wealth tax on $1.2 trillion = $60 billion tax bill, each.
That's 50% of their actual Alphabet holdings—wiped out by a "5%" tax.
Section 50303(c)(3)(C) of the 2026 Billionaire Tax Act states: "For any interests that confer voting or other direct control rights, the percentage of the business entity owned by the taxpayer shall be presumed to be not less than the taxpayer's percentage of the overall voting or other direct control rights."
This means if a founder holds shares representing only 3% of economic interest but 30% of voting control (through Class B supervoting shares), the tax would presume their ownership stake is at least 30% for valuation purposes, not 3%.
The wealth tax is poorly defined and designed to drive tech innovation out of California.
california bans plastic bag to 'save the planet', but now every paper bag requires 3x more energy to produce, 3x more trees to chop, 3x more fossils to burn, and 3x the proof of how incompetent this state is. oh, and btw, your take out got wet.























