Expression, purification, and function of baculovirus infected insect cells‐derived hookworm AIP‐1 and AIP‐2 proteins

Author:

Lee Chae Eun1,Chung Hyun Joo1,Lee Da Won1,Lim Jong Seok1ORCID,Lee Jeong Hwan2,Ko Kisung2ORCID,Hong Soon Auck3,Hong Min Eui3,Kim Joo Young3,Lee Hye Jun4,Kim Jin Wook56,Myung Soon Chul1ORCID

Affiliation:

1. Department of Urology, College of Medicine Chung‐Ang University Seoul Republic of Korea

2. Department of Medicine, BioSystems Design Lab, College of Medicine Chung‐Ang University Seoul Republic of Korea

3. Department of Pathology, Chung‐Ang University Hospital, College of Medicine Chung‐Ang University Seoul Republic of Korea

4. Department of Family Medicine, Chung‐Ang University Hospital, College of Medicine Chung‐Ang University Seoul Republic of Korea

5. Department of Urology Chung‐Ang University Gwangmyeong Hospital Gwangmyeong Gyeonggi‐do Republic of Korea

6. Department of Medical Informatics, College of Medicine Chung‐Ang University Seoul Republic of Korea

Abstract

AbstractAnti‐inflammatory protein (AIP)‐1 and AIP‐2, identified as parasite excretory/secretory (ES) proteins, play a crucial role in promoting the survival of the parasite and evading the host immunological response. Both proteins inhibit inflammatory reactions, induce apoptosis in effector cells, and influence the phenotype of the immune response. Numerous parasite‐derived proteins have shown promise as therapeutic targets for inflammatory and allergic diseases. Despite this, the precise biological roles, and molecular characteristics of many such proteins remain unclear.In this study, AIP‐1 and AIP‐2 were produced in the baculovirus‐insect cell expression system (BEVS). The multiplicity of infection (MOI) and the duration of infection conditions for AIP‐1 and AIP‐2 protein expression were successfully optimized to induce the highest expression levels of AIP‐1 and AIP‐2 proteins in insect cells. The insect cell‐derived AIP‐1 and AIP‐2 exhibited inhibitory functions against human matrix metalloproteinases (MMPs). This study demonstrates that insect cell‐derived AIP‐1 and AIP‐2 have the potential as therapeutic proteins for MMP‐TIMP (Metalloprotease‐Tissue inhibitor of metalloprotease) axis related disease.

Funder

National Research Foundation of Korea

Publisher

Wiley

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