# Handshaking for ultrafast endocytosis: Dynamin1xA and Endophilin A1 sealed the deal

**Authors:** Santiago López-Begines, Rafael Fernández-Chacón

PMC · DOI: 10.1038/s44318-024-00179-1 · The EMBO Journal · 2024-07-23

## TL;DR

This study explains how neurons can rapidly recycle synaptic components through preassembled protein machinery.

## Contribution

The paper discovers a novel interaction between Dynamin1xA and Endophilin A1 that enables ultrafast endocytosis.

## Key findings

- A regulated interaction between Dynamin1xA and Endophilin A1 was identified.
- This interaction supports preassembled machinery for ultrafast endocytosis at synapses.

## Abstract

Brain function relies on quick inter-neuron communication at specialized points of contact termed synapses. In the latest issue of The EMBO Journal, Imoto, Xue, et al (2024) report the discovery of a novel, regulated interaction between two major endocytosis players which supports the notion of a preassembled protein machinery at presynaptic nerve terminals that can explain how the high speed of ultrafast endocytosis is possible.

A new study reveals how preassembled components at the endocytic zone permit ultrafast endocytosis to occur so quickly.

## Full-text entities

- **Genes:** SH3GL2 (SH3 domain containing GRB2 like 2, endophilin A1) [NCBI Gene 6456] {aka CNSA2, EEN-B1, SH3D2A, SH3P4}

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11329764/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC11329764/full.md

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Source: https://tomesphere.com/paper/PMC11329764