# Identification of a Novel Peptide from Agaricus blazei Murrill and Its Immune-Enhancing Activity by Regulation of PI3K/AKT/mTOR Signaling Pathways in RAW 264.7 Cells

**Authors:** Xianguo Zou, Yeqi Yu, Yun Chi, Kai Yang, Zeyuan Deng, Hong Gu, Peilong Sun

PMC · DOI: 10.3390/foods14203467 · Foods · 2025-10-11

## TL;DR

A new peptide from Agaricus blazei Murrill boosts immune activity in macrophage cells by affecting key signaling pathways.

## Contribution

The novel peptide LNEDELRDA is identified as a potential food-borne immunomodulator through its effect on PI3K/AKT/mTOR pathways.

## Key findings

- LNEDELRDA peptide showed strong immune-enhancing activity in RAW 264.7 cells.
- Peptide binding to PI3K, AKT, mTOR, and cytokines was confirmed with specific binding energies.
- Peptide increased cell viability, phagocytic activity, and cytokine production in macrophages.

## Abstract

This study aimed to screen and identify a novel immune-enhancing peptide and explore the molecular mechanism. Five novel peptides were identified from Agaricus blazei Murrill (ABM), and their secondary structure components consisted of random coil (50.5%), α-helix (28.9%), β-turn (15.6%), and β-sheet (5.0%). A novel peptide (LNEDELRDA) with a molecular weight of 1074.0989 Da could bind with PI3K, AKT, mTOR, IL-6, IL-1β, and TNF-α through hydrogen bonding interactions, and the binding energies were −8.1, −8.3, −7.2, −6.0, −7.4, and −5.8 kcal/mol, respectively. This peptide was synthesized and validated for immune-enhancing ability, showing the strongest immune-enhancing capacity by increasing the cell viability and phagocytic activity of RAW 264.7 macrophages, significantly promoting the production of NO, cytokines TNF-α, IL-1β, and IL-6 in cells, and up-regulating the mRNA and protein expression levels of the PI3K/AKT/mTOR signaling pathway. Our results are the first to reveal that ABM-derived peptide LNEDELRDA could be considered as a promising food-borne immunomodulator that could contribute to enhancing immune function.

## Linked entities

- **Proteins:** PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha), AKT1 (AKT serine/threonine kinase 1), MTOR (mechanistic target of rapamycin kinase), IL6 (interleukin 6), IL1B (interleukin 1 beta), TNF (tumor necrosis factor)

## Full-text entities

- **Genes:** Pik3r1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 18708] {aka PI3K, p50alpha, p55alpha, p85alpha}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Mtor (mechanistic target of rapamycin kinase) [NCBI Gene 56717] {aka 2610315D21Rik, FRAP, FRAP2, Frap1, RAFT1, RAPT1}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}
- **Chemicals:** LNEDELRDA (-), NO (MESH:D009614)
- **Cell lines:** RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12564683/full.md

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12564683/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12564683/full.md

---
Source: https://tomesphere.com/paper/PMC12564683