# TcSERPIN, an inhibitor that interacts with cocoa defense proteins and has biotechnological potential against human pathogens

**Authors:** Monaliza Macêdo Ferreira, Keilane Silva Farias, Maria Zugaib, Akyla Maria Martins Alves, Geiseane Velozo Amaral, Maria Luíza do Carmo Santos, Andria dos Santos Freitas, Brenda Conceição Guimarães Santana, Sérgio Liberato dos Santos Júnior, Irma Yuliana Mora-Ocampo, Ariana Silva Santos, Marcelo Fernandes da Silva, Bruno Silva Andrade, Carlos Priminho Pirovani

PMC · DOI: 10.3389/fpls.2024.1337750 · Frontiers in Plant Science · 2024-01-29

## TL;DR

This study identifies TcSERPIN, a protease inhibitor from cocoa, which shows promise for biotechnology and plant defense against pathogens.

## Contribution

Characterization of TcSERPIN from Theobroma cacao and its potential as a biotechnological tool against human pathogens and plant diseases.

## Key findings

- TcSERPIN inhibits papain and trypsin proteases, showing potential for pest and pathogen control.
- TcSERPIN captures endogenous defense proteins from cocoa, linked to stress and metabolic pathways.
- TcSERPIN and TcCYS4 reduce geohelminth larvae movement, indicating biotechnological application potential.

## Abstract

In plants, serpins are a superfamily of serine and cysteine protease inhibitors involved in stress and defense mechanisms, with potential for controlling agricultural pests, making them important biotechnological tools. The objective of this study was to characterize a serpin from Theobroma cacao, called TcSERPIN, to identify its endogenous targets and determine its function and biotechnological potential. TcSERPIN has 390 amino acid residues and shows conservation of the main active site, RCL. Cis-elements related to light, stress, hormones, anaerobic induction, cell cycle regulation and defense have been identified in the gene’s regulatory region. TcSERPIN transcripts are accumulated in different tissues of Theobroma cacao. Furthermore, in plants infected with Moniliophtora perniciosa and Phytophthora palmivora, the expression of TcSERPIN was positively regulated. The protein spectrum, rTcSERPIN, reveals a typical β-sheet pattern and is thermostable at pH 8, but loses its structure with temperature increases above 66°C at pH 7. At the molar ratios of 0.65 and 0.49, rTcSERPIN inhibited 55 and 28% of the activity of papain from Carica papaya and trypsin from Sus scrofa, respectively. The protease trap containing immobilized rTcSERPIN captured endogenous defense proteins from cocoa extracts that are related to metabolic pathways, stress and defense. The evaluation of the biotechnological potential against geohelminth larvae showed that rTcSERPIN and rTcCYS4 (Theobroma cacao cystatin 4) reduced the movement of larvae after 24 hours. The results of this work show that TcSERPIN has ideal biochemical characteristics for biotechnological applications, as well as potential for studies of resistance to phytopathogens of agricultural crops.

## Linked entities

- **Proteins:** LOC110813108 (papain-like), prss1.L (serine protease 1 L homeolog)
- **Species:** Theobroma cacao (taxon 3641), Carica papaya (taxon 3649), Sus scrofa (taxon 9823)

## Full-text entities

- **Species:** Carica papaya (mamon, species) [taxon 3649], Theobroma cacao (cacao, species) [taxon 3641], Homo sapiens (human, species) [taxon 9606], Phytophthora palmivora (species) [taxon 4796], Sus scrofa (pig, species) [taxon 9823]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10859438/full.md

## References

88 references — full list in the complete paper: https://tomesphere.com/paper/PMC10859438/full.md

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Source: https://tomesphere.com/paper/PMC10859438