# β‑Hairpin Antimicrobial Peptides: Class Diversity and Sequence Analysis

**Authors:** Rabina Ramtel, Richard Gu, Mutiat A. Abdulkareem, Justin R. Randall

PMC · DOI: 10.1021/acsinfecdis.5c01055 · ACS Infectious Diseases · 2026-02-02

## TL;DR

This paper reviews and analyzes β-hairpin antimicrobial peptides, highlighting their unique structure and properties, and suggests ways to expand their discovery and use.

## Contribution

The paper identifies 27 unique β-hairpin antimicrobial peptide families and provides insights into their sequence characteristics for future development.

## Key findings

- β-hairpin antimicrobial peptides are characterized by lengths of 11–25 amino acids and a cationic charge.
- They contain two or more cysteine pairs and show strong enrichment for arginine over lysine.
- The paper emphasizes strategies to expand the class and improve its underrepresentation.

## Abstract

Interest in antimicrobial peptides has increased dramatically over the last few decades as researchers continue to explore their potential as alternatives to small molecules, as well as their applications in agriculture and food preservation. One promising yet small antimicrobial peptide class is that consisting of a single β-hairpin cyclized via intramolecular disulfide bonds, commonly termed β-hairpin antimicrobial peptides (β-AMPs). Their short length constrained cyclic structure and wide range of activities make them exciting to the general scientific community and drug developers alike; however, despite being found across several phyla, there remain fewer than 30 identified sequence families, making them exceedingly rare relative to more common structural classes. In this review, we identify and describe 27 unique macrocyclic β-AMP sequence families from the literature, with an emphasis on newer and lesser-known families. We then analyze the class’s sequence composition both as a whole and broken down by structural region, finding common characteristics including lengths of 11–25 amino acids, cationic charge, two or more cysteine pairs separated by at least three residues, and strong enrichment for arginine relative to lysine. We then discuss strategies for using these sequence characteristics to help expand the class and improve their relative underrepresentation.

## Full-text entities

- **Chemicals:** Peptides (MESH:D010455), beta-AMP (-), disulfide (MESH:D004220)

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13001179/full.md

## References

130 references — full list in the complete paper: https://tomesphere.com/paper/PMC13001179/full.md

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Source: https://tomesphere.com/paper/PMC13001179