Latent Space ★ 78 4 min

Why AlphaFold Didn't Solve Protein Folding — Pushmeet Kohli, Google DeepMind & Sal Candido, Biohub

🔗 https://www.latent.space/p/biohub-deepmind

📌 Google DeepMind × Biohub 對談:AlphaFold 其實沒解決蛋白質摺疊問題

TL;DR:DeepMind 的 Pushmeet Kohli 與 Biohub 的 Sal Candido 在 Latent Space 專題對談中指出,AlphaFold 只解開了靜態結構預測,蛋白質動態、設計與全細胞建模仍是未竟之業。

AlphaFold 拿下諾貝爾化學獎、被譽為結構生物學的里程碑,但如果你問兩位真正在第一線做蛋白質 AI 的研究者「蛋白質摺疊問題解決了嗎?」,得到的答案居然是「還沒」。這場由 Brandon Anderson 主持的對談,把這個反直覺的結論拆解得相當細。

🤔 資料界也有「苦澀的教訓」嗎?

主持人開場就拋出一個改寫版的 Bitter Lesson:如果 Rich Sutton 說「能夠規模化的方法終將勝出」,那麼資料是否也存在同樣的規律?Sal Candido 的回答很務實:scaling law 不是處處都有,真正的工作是先找出「放更多運算、更多資料進去,就能得到更好結果」的那個情境,一旦找到,問題就變成工程問題,可以「轉動把手」持續優化。但前提是資料本身要帶有解決目標問題所需的資訊與統計特性,否則模型終究無法超越資料本身去泛化。

🧩 低品質的 metagenomic 資料,反而讓蛋白質語言模型更強

Sal 坦承自己做研究傾向「挑現成資料來用」,這有好有壞。壞處是容易導向「什麼資料好生成就規模化什麼資料」的懶惰路線;好處則是常有意外收穫——他舉例,用 metagenomic 序列(很多甚至不是完整、真實的蛋白質)訓練蛋白質語言模型,結果卻提升了模型在設計真實可用蛋白質、理解已知蛋白質上的表現。他認為真正該問的問題不是「有什麼資料」,而是「解決這個問題到底需要什麼資料」,這也是 Biohub 強調社群開放協作的原因:只有建模者、資料生成者和科學社群一起工作,才能真正定義出需要的資料,進而找到對的 scaling law。

Pushmeet Kohli 則從 DeepMind 內部視角回應:他當年在 DeepMind 聽 Rich Sutton 親自講這堂課時,體會到的重點並非「資料是否有用」這種具體層面的問題,而是更概念性、更根本的東西。

💡 AlphaFold 到底還沒解決什麼

根據節目議程,兩人進一步談到 AlphaFold 手工設計的架構與科學直覺在其中的角色,以及「好資料勝過單純堆資料量」的設計哲學。更關鍵的是,對談明確點出 AlphaFold 並未真正解決整個蛋白質摺疊問題——靜態結構預測只是故事的一部分,蛋白質的動態行為(dynamics)、無序區域(disorder)都還在靜態結構預測的能力範圍之外。節目也提到 cryo-EM 顯微影像可能是解鎖更豐富生物表徵的下一個入口,以及建模視角需要從「單一蛋白質」擴展到「完整生物系統」,這正是打造 virtual cell(虛擬細胞)的核心挑戰。

此外議程也涵蓋了蛋白質語言模型中可能藏有尚未被解鎖的科學知識、可信度與不確定性校準為何比完全可解釋性更重要,以及未來前沿模型是否可能比人類更擅長理解其他 AI 系統等議題。

🎯 對 AI 研究者的啟示

這場對談給做生物 AI 的工程師一個提醒:盲目堆大模型、堆算力不是終點,找到「對的 scaling law」與「對的資料」才是真正的工程槓桿。而像 Biohub 這樣強調「以社群協作定義需求、而非被現有資料牽著走」的做法,也值得其他領域的 AI 團隊借鏡。

🔗 來源

#AlphaFold #ProteinFolding #GoogleDeepMind #Biohub #ScalingLaws #BitterLesson #ProteinLanguageModel #VirtualCell #AIforScience #DrugDiscovery

原始資料 Latent Space · 收集於 2026-10-10
來源原標題
Why AlphaFold Didn't Solve Protein Folding — Pushmeet Kohli, Google DeepMind & Sal Candido, Biohub
作者
Latent Space
原始標籤
blog
原始連結
https://www.latent.space/p/biohub-deepmind

摘要原文

From the Bitter Lesson of AI scaling to the unsolved mysteries of protein folding , Google DeepMind’s Pushmeet Kohli and Biohub’s Sal Candido are rethinking what it takes to build AI that truly understands biology. In this special panel moderated by Brandon Anderson , they explore why AlphaFold’s breakthrough was only the beginning , why scaling compute and data alone won’t solve biology, and how the next generation of AI models could transform our understanding of proteins, cells, and human disease. We go deep on the future of AI-driven biology : finding scaling laws in biological data, the tradeoffs between scientific intuition and general-purpose architectures, why protein structure prediction is far from solved, and what it would take to build predictive models of living systems. Pushmeet reflects on the lessons behind AlphaFold , the limits of human interpretability, and whether future frontier models could understand other AI systems better than we can. Sal explains why protein language models may already contain scientific knowledge we haven’t unlocked, how biological modeling must move beyond individual proteins, and why achieving Biohub’s mission to cure all disease requires thinking in terms of 10x breakthroughs rather than incremental improvements. The Bitter Lesson for biology : why scaling compute and data isn’t enough Why finding the right scaling law matters more than blindly increasing model size How low-quality metagenomic data can improve protein language models Why AI researchers optimize for available data instead of the most important scientific problems Lessons from DeepMind on balancing modeling, data generation, and scientific expertise Why building a virtual cell requires fundamentally different datasets AlphaFold’s handcrafted architecture and the role of scientific intuition Why good data matters more than simply having more data Inductive biases, scaling laws, and the future of specialized AI architectures Why we aren’t in a post-Transformer world , but architectures are evolving Why AlphaFold didn’t actually solve all of protein folding Protein dynamics, disorder , and the limitations of static structure prediction How cryo-EM micrographs could unlock richer biological representations Moving from models of individual proteins to whole biological systems Feynman’s famous principle and why AI can now create things we don’t understand The hidden biological knowledge inside protein language models Why trustworthiness and uncertainty calibration matter more than full interpretability Whether frontier AI models could interpret other AI systems better than humans When AI could deliver 10x–100x acceleration in drug discovery Why curing all disease requires thinking about 10x breakthroughs instead of 10% improvements LinkedIn: https://www.linkedin.com/in/pushmeet-kohli-4838994/ Biohub: https://biohub.org/team/salvatore-candido/ LinkedIn: https://www.linkedin.com/in/salcandido/ LinkedIn: https://www.linkedin.com/in/brandon--anderson 00:00:00 Introduction: The Bitter Lesson for Biological Data 00:01:00 Finding Scaling Laws and the Right Data for Biology 00:04:54 DeepMind’s Bitter Lesson: Solving Problems vs. Scaling Models 00:06:50 AlphaFold, Data Limitations, and Building the Virtual Cell 00:09:52 Handcrafted Architectures vs. Scaling Compute 00:11:53 Good Data, Inductive Bias, and Model Design 00:13:39 Beyond Transformers: The Future of AI Architectures 00:14:38 Why AlphaFold Hasn’t Solved Protein Folding 00:17:39 Protein Dynamics, Design, and Cryo-EM 00:19:09 From Individual Proteins to Whole Biological Systems 00:20:43 Feynman’s Principle: Creating Without Understanding 00:22:18 The Hidden Knowledge Inside Protein Language Models 00:23:48 AlphaFold, Trustworthiness, and Interpretability 00:25:56 Could AI Understand Other AI Models Better Than Humans? 00:27:43 When Will AI Revolutionize Drug Discovery? 00:29:47 Why Curing All Disease Requires 10x Breakthroughs Brandon Anderson [00:00:04]: Great to be here. What an exciting morning. So many cool announcements. I think the future of bioscience is being announced right here. This is the modeling session. We’re all modelers, so of course it’s natural for us to talk about data. One of the things I like to think about when it comes to data is how to scale it properly. This has brought me to the question of the bitter lesson, but recast in the frame of data. The bitter lesson, for those of you who are not AI people, is the statement that methods that scale win eventually. If you can scale enough, it wins. So my question, starting with Sal, is: Is there a bitter lesson for data? Sal Candido [00:01:00]: For sure. You obviously need the right data in order for it to work. One misconception of scaling laws is that scaling laws are everywhere and they always exist. A lot of the work is actually finding that scaling law. A lot of what we do is trying to figure out: What’s a situation where, if you put more compute into it, if you put more data into it, you get a better result out? That’s a great situation because, once that happens, you can turn the crank. It becomes an engineering problem, which is something I like. That has to do with architecture, but it also very much has to do with data. If you don’t have data with the right information and statistics to solve the problem you want, you’re not going to get a model that has the capabilities and understanding you want. You can only really pull information from the data you have and use that to generalize beyond it. Brandon Anderson [00:02:09]: When it comes to data collection, how do you think about which modalities are best? A related question: Do modelers tend to work on problems where the data is available, rather than the problems that best serve their goals or have the greatest impact on translational medicine? Sal Candido [00:02:32]: For sure. I won’t speak for all modelers, but I’m lazy, so I’m going to work with what’s available. There’s a good side and a bad side to this. The good side is that, when you’re doing conventional machine learning, you’re often looking for the most pristine, high-quality data examples you can find. But if you’re like me, you’re rooting around in the back room, looking through people’s junk to see what’s there. A concrete example is training a protein language model on metagenomic sequences, which are not the highest-quality data. In fact, much of that data, I can guarantee you, isn’t even a real, whole protein. And yet it makes the performance of the model go up for designing real proteins that work and understanding proteins that we know exist. That’s the positive side. But it can lead you to a negative place where you say, “Let’s just scale up the data that we can generate easily.” I don’t think that’s necessarily the way to do it. That’s one of the things that’s exciting to me about what we’re talking about here today with the BBI. It’s going out and asking, “What is the data that we need to solve the problem?” It’s about the right resources, but also the right community. One thing we try to do at Biohub is work in the open, work with the community, and move the whole community forward. That’s critical because, if you just have people building models, we’re going to lean toward the data that exists. If you just have people generating data, they’re going to lean toward the things that can be generated. But if you can work together as a community, every step of the way, in an open fashion, you can figure out what data you actually need. Then you can find that scaling law. Brandon Anderson [00:04:50]: Pushmeet, what do you think about the bitter lesson for data? Pushmeet Kohli [00:04:54]: I was at DeepMind when Rich was with us and thinking about this idea of the bitter lesson. What I took from Rich’s original lecture at DeepMind wasn’t about the specific notion of whether data is useful or how we should think about machine learning. My take was that he was talking about something more conceptual.

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