Cells produce thousands of proteins every day. Sometimes, due to mutations, heat shock, or oxidative stress, proteins get misfolded. When this happens, the cell usually tries to degrade them using the ubiquitin-proteasome system. But when that system is overloaded, misfolded proteins start sticking together and forming toxic aggregates.

To protect itself, the cell bundles these into a structure called an aggresome. That’s where aggrephagy steps in: a special form of autophagy designed to remove these aggregates. But aggrephagy doesn't just happen on its own it needs a signal.

Researchers have identified a key enzyme (often HDAC6 or similar molecules) that plays the role of a cleanup coordinator. This enzyme does three essential things:

1. Senses Trouble: It binds to misfolded proteins that have been tagged with ubiquitin, a molecular "trash label."
2. Mobilizes Machinery: It brings in other proteins that help move the aggresome to the right spot in the cell.
3. Starts Autophagy: It helps recruit the autophagy machinery proteins like p62 and LC3 to build the membrane that will enclose and destroy the aggresome.

Without this enzyme, the entire cleanup process fails to start. Misfolded proteins stay in the cell, building up and eventually damaging it.

This enzyme acts like a first responder in the cell’s stress management system. It doesn’t just react it decides when and where to launch a targeted cleanup.

Understanding this enzyme gives scientists a clearer picture of:

• How cells protect themselves under stress
• Why some cells fail to clear aggregates in disease
• New strategies to enhance the cell's natural defenses

This is especially important in neurodegenerative diseases, where misfolded proteins are a major problem. Boosting this enzyme’s activity might help prevent cells from being overwhelmed.