# AP2: an indispensable host factor in virus infection

**Authors:** Rui Li, Yan Jiang, Xinrong Wang, Longxiang Zhang, Yue Wang

PMC · DOI: 10.1128/jvi.02164-25 · Journal of Virology · 2026-01-21

## TL;DR

This paper reviews how the host protein AP2 is used by viruses during infection and how targeting it could lead to broad-spectrum antiviral treatments.

## Contribution

The paper provides a comprehensive synthesis of AP2's roles in the viral life cycle and its potential as a target for antiviral therapies.

## Key findings

- AP2 is exploited by viruses at multiple stages of their life cycle, including entry, replication, and immune evasion.
- Targeting AP2 and its pathways offers a promising approach for developing broad-spectrum antiviral strategies.
- AP2 serves as a critical host-pathogen interface, influencing viral pathogenesis and drug discovery.

## Abstract

Adaptor protein complex 2 (AP2), a central regulator of clathrin-mediated endocytosis and intracellular cargo trafficking, is hijacked by numerous viruses to complete their infectious cycles. This review systematically synthesizes the multifaceted roles of AP2 across the entire viral life cycle, from entry and replication to assembly and release, as well as in immune evasion. By delineating how diverse viruses exploit this key host machinery, we further consolidate the rationale and current progress in developing broad-spectrum antiviral strategies that target AP2 and its regulatory pathways. This work aims to provide a unified perspective on AP2 as a critical host-pathogen interface, offering new insights into viral pathogenesis and antiviral drug discovery.

## Linked entities

- **Proteins:** FABP4 (fatty acid binding protein 4)

## Full-text entities

- **Genes:** TFAP2A (transcription factor AP-2 alpha) [NCBI Gene 7020] {aka AP-2, AP-2alpha, AP2TF, BOFS, TFAP2}
- **Diseases:** virus infection (MESH:D014777)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12911872/full.md

## References

234 references — full list in the complete paper: https://tomesphere.com/paper/PMC12911872/full.md

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Source: https://tomesphere.com/paper/PMC12911872