# AlphaFold 揭示心脏病关键蛋白结构

- 来源：Google DeepMind：Blog（RSS）
- 发布时间：2025-11-25 23:52
- AIHOT 链接：https://aihot.virxact.com/items/cmnwsdqal003uslagd8hbhly7
- 原文链接：https://deepmind.google/blog/revealing-a-key-protein-behind-heart-disease

## AI 摘要

AlphaFold 成功解析了一种与心脏病相关的关键蛋白质结构，为理解疾病分子机制提供重要依据。该突破有助于加速心血管疾病相关药物的研发进程。

## 正文

AlphaFold Reveals a Key Protein Behind Heart Disease — Google DeepMind

November 25, 2025 Science

Revealing a key protein behind heart disease

- [x]

Credit: MolGraphics.com / Zachery Bernsden and Keith Cassidy

In a breakthrough powered by AlphaFold, scientists have mapped the structure of the large protein that gives “bad cholesterol” its form – a discovery that could help transform how researchers and clinicians treat the world’s leading cause of death

The race to reveal a key protein behind heart disease has long been both an important public health goal and a stubborn scientific problem.

For assistant professors Zachary Berndsen and Keith Cassidy at the University of Missouri (Mizzou), it was also personal. Both have a family history of heart disease – a reminder of what’s at stake in their work to better understand and ultimately help treat this deadly condition.

“For 50 years, people have wanted to see what this protein looked like,” says Berndsen.

That protein, apoB100, has defied mapping not only because it’s enormous (for a protein), but also because it connects to fats and other molecules in complicated ways. ApoB100 forms the molecular scaffold of “bad cholesterol”, which is known to scientists as low-density lipoprotein (LDL).

LDL is the major carrier of fat through the bloodstream and a key risk factor for atherosclerotic cardiovascular disease (ASCVD), the world’s leading cause of death. Discovering the structure of its key protein promised to shed light on how bad cholesterol becomes harmful inside the body, giving scientists a better chance to develop ways to prevent and treat ASCVD. AlphaFold is playing a central role in this effort.

At Mizzou, biochemist Berndsen first used cryo-electron microscopy (cryo-EM) to capture images of LDL particles. The images weren’t sharp enough to map the structure of apoB100 with atomic precision, so Berndsen’s physicist collaborator, Cassidy, turned to AlphaFold. He used it to generate atomic-resolution predictions of the protein’s structure and then refined those predicted shapes by comparing them against the cryo-EM image data.

Coming at the problem using both cryo-EM microscopy and Alphafold is what unlocked this breakthrough, says Cassidy: “AlphaFold played a profound role in this discovery, providing the raw material to interpret our experimental structure in a way that was frankly impossible before.”

The resulting model revealed bad cholesterol’s key protein in remarkable detail: a cage-like shell that wraps around each LDL particle, including a ribbon-like belt that keeps the particle intact in the bloodstream. Knowing this structure opens new possibilities for preventing, diagnosing and treating high cholesterol and ASCVD, including therapies that could target LDL more precisely. The potential benefit to global health is hard to overstate.

While such applications will take time, revealing the structure of apoB100 is a landmark achievement, and a deeply satisfying one for Berndsen. “It was the first structure I ran through AlphaFold the week it became available, and the first protein I wanted to look at with our two-storey cryo-EM machine,” he says. “Solving the structure of apoB100 was a dream come true.”

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