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Anthropic宣布Claude主导发现新型基因编辑机制

Today we announced the Claude-led discovery of a molecular machine that we suspe…

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这是AI从纯数字领域向实体科学跨越的关键里程碑,展示了模型在复杂科研闭环中的核心驱动力,值得所有关注AGI落地场景的研究者关注。

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.

今天我们宣布,由 Claude 主导发现了一种分子机器,我们怀疑它可能代表一种新的基因编辑机制。其精确功能、生物技术效用(如果有的话)或重要程度尚不清楚,但至少可以说,作为一名博士生,我会为完成这项工作而感到自豪。这项工作主要由 Claude 完成,尽管并非完全由其独立完成:我们的生命科学团队提出了一项广泛的研究方向,Claude 阅读了相关文献和大量基因组数据并发现了有趣的内容,随后 Claude 提出了验证该发现的实验方案,由我们的团队执行了这些实验。

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.

人们很容易将此视为一次性的事件或单纯的奇闻异事,但我们反复观察到一种模式:人工智能在新智力领域的表现会在短短几年内从薄弱发展到超越人类水平。2023年,模型在达到普通高中生水平的数学问题上仍感到吃力;2024年,它们开始在全国顶尖高中生的数学竞赛中表现出色;2025年,它们开始解决一些次要的开放性问题;2026年初,它们开始解决更重要的开放性问题;而在2026年底,它们开始解决数学领域最顶尖的几个开放性问题。我们相信,AI 在生物学领域也遵循类似的指数增长趋势。

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).

当然,生物学与数学的主要区别在于,数学可以纯粹通过理论推导完成,而生物学则需要实验验证。有人据此得出结论,认为 AI 在生物学中的效用将受到限制。我们认为这是错误的。正如我们今天所展示的,人类可以与 AI 协作进行实验,在几周内验证关键结果,并在必要时与 AI 合作对其发现进行迭代优化。最终,甚至有可能让 Claude 本身在具备适当安全措施的前提下,通过自主控制实验室设备来安全地执行实验,但我们今天并未这样做(我们的实验室也是 BSL1/BSL2 设施,不处理对人类危险的材料)。

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.

更广泛地说,生物医学进步包含多个阶段——从基础生物学发现,到转化研究,再到药物发现、临床试验,最终将药物和医疗保健实际交付给患者。我们也对这些后期阶段感兴趣,但即便只是加速基础生物学发现这一第一阶段,也有潜力加快并拓宽整个流程。改善我们对生物学的理解并增强生物学家的工具,可以推动所有后续阶段的发展,例如识别新的药物靶点、发现新的治疗方式、实现更精确的测量,以及加速实验循环,而实验循环本身又会进一步加速我们对生物学的理解。这本身不会缩短临床试验的时间,但如果成功,它可能会大幅增加进入流程的有前景候选药物的数量——即在延迟不变的情况下提高吞吐量。

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.

在《慈爱机器》(Machines of Loving Grace)一书中,我写道 AI 有可能“在5-10年内治愈大多数疾病”——这一目标听起来似乎不可能,但我相信,如果将 AI 应用于流程的每一个阶段,这一目标仅仅是勉强可行的。第一步是证明 AI 首先能够帮助并最终驱动生物学发现。

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.

Claude 的发现是数十年来一系列相关前期工作的最新成果,始于 CRISPR 等系统,并延续至近年来发现的桥接重组酶(bridge recombinase)和 VIPR。最近,人们对基于逆转录酶(RT)的系统兴趣日益浓厚,该酶正是 Claude 所识别系统的基础。而在最近,斯坦福大学的一个独立团队描述了一种新型 RT 系统及其相关的非编码阵列,该系统在某些方面与 Claude 发现的系统相似,尽管它们是各自独立演化的不同系统。我相信我们正处于发现此类系统并将其开发为生物技术强大工具的开端。

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.

我为 Anthropic 投入资源以通过生命科学加速 AI 的公共效益感到自豪,我们的目标既是扩大生命科学团队规模,也是与其他科学家合作,将此方法扩展到更广泛的问题领域。如果您有研究合作的提案,或有兴趣加入我们的生命科学团队,请随时联系。

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