# Searching for EGF Fragments Recreating the Outer Sphere of the Growth Factor Involved in Receptor Interactions

**Authors:** Katarzyna Czerczak-Kwiatkowska, Marta Kaminska, Justyna Fraczyk, Ireneusz Majsterek, Beata Kolesinska

PMC · DOI: 10.3390/ijms25031470 · International Journal of Molecular Sciences · 2024-01-25

## TL;DR

This study identifies EGF fragments that interact with the EGF receptor and are non-toxic, potentially useful in medicine.

## Contribution

A novel method using peptide microarrays and SPOT technique to identify functional EGF fragments is introduced.

## Key findings

- EGF fragments with high affinity for the EGF receptor were successfully identified.
- The selected EGF fragments showed no cytotoxicity in biological tests.
- The method can be applied to study protein–peptide interactions and has potential medical applications.

## Abstract

The aims of this study were to determine whether it is possible to use peptide microarrays obtained using the SPOT technique (immobilized on cellulose) and specific polyclonal antibodies to select fragments that reconstruct the outer sphere of proteins and to ascertain whether the selected peptide fragments can be useful in the study of their protein–protein and/or peptide–protein interactions. Using this approach, epidermal growth factor (EGF) fragments responsible for the interaction with the EGF receptor were searched. A library of EGF fragments immobilized on cellulose was obtained using triazine condensing reagents. Experiments on the interactions with EGFR confirmed the high affinity of the selected peptide fragments. Biological tests on cells showed the lack of cytotoxicity of the EGF fragments. Selected EGF fragments can be used in various areas of medicine.

## Linked entities

- **Proteins:** EGF (epidermal growth factor), EGFR (epidermal growth factor receptor)

## Full-text entities

- **Genes:** EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** cytotoxicity (MESH:D064420)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC10855902/full.md

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10855902/full.md

## References

105 references — full list in the complete paper: https://tomesphere.com/paper/PMC10855902/full.md

---
Source: https://tomesphere.com/paper/PMC10855902