Proteomics of the 26S proteasome in Spodoptera frugiperda cells infected with the nucleopolyhedrovirus, AcMNPV

• Published in: Biochimica et biophysica acta Vol. 1864; no. 6; pp. 738 - 746
• Main Authors: Lyupina, Yulia V., Zatsepina, Olga G., Serebryakova, Marina V., Erokhov, Pavel A., Abaturova, Svetlana B., Kravchuk, Oksana I., Orlova, Olga V., Beljelarskaya, Svetlana N., Lavrov, Andrey I., Sokolova, Olga S., Mikhailov, Victor S.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.06.2016
• Subjects: 20S proteasome; 26S proteasome; AcMNPV; Amino Acid Sequence; Animals; Autographa californica; Baculovirus; Cell Line; Electrophoresis, Gel, Two-Dimensional; Lepidoptera; Molecular Sequence Data; Nuclear polyhedrosis virus; Nucleopolyhedrovirus; Nucleopolyhedrovirus - pathogenicity; Proteasome Endopeptidase Complex - chemistry; Proteomics; Sequence Homology, Amino Acid; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Spodoptera - cytology; Spodoptera frugiperda; Nucleopolyhedrovirus; Spodoptera frugiperda; 26S proteasome; 20S proteasome; AcMNPV; Baculovirus
• ISSN: 1570-9639; 0006-3002; 1878-1454
• DOI: 10.1016/j.bbapap.2016.02.021

Baculoviruses are large DNA viruses that infect insect species such as Lepidoptera and are used in biotechnology for protein production and in agriculture as insecticides against crop pests. Baculoviruses require activity of host proteasomes for efficient reproduction, but how they control the cellular proteome and interact with the ubiquitin proteasome system (UPS) of infected cells remains unknown. In this report, we analyzed possible changes in the subunit composition of 26S proteasomes of the fall armyworm, Spodoptera frugiperda (Sf9), cells in the course of infection with the Autographa californica multiple nucleopolyhedrovirus (AcMNPV). 26S proteasomes were purified from Sf9 cells by an immune affinity method and subjected to 2D gel electrophoresis followed by MALDI-TOF mass spectrometry and Mascot search in bioinformatics databases. A total of 34 homologues of 26S proteasome subunits of eukaryotic species were identified including 14 subunits of the 20S core particle (7 α and 7 β subunits) and 20 subunits of the 19S regulatory particle (RP). The RP contained homologues of 11 of RPN-type and 6 of RPT-type subunits, 2 deubiquitinating enzymes (UCH-14/UBP6 and UCH-L5/UCH37), and thioredoxin. Similar 2D-gel maps of 26S proteasomes purified from uninfected and AcMNPV-infected cells at 48hpi confirmed the structural integrity of the 26S proteasome in insect cells during baculovirus infection. However, subtle changes in minor forms of some proteasome subunits were detected. A portion of the α5(zeta) cellular pool that presumably was not associated with the proteasome underwent partial proteolysis at a late stage in infection. •26S proteasome was purified from fall armyworm Spodoptera frugiperda Sf9 cells.•Subunits of 26S proteasome from Sf9 cells were identified by proteomic analysis.•Infection with baculovirus AcMNPV did not affect the structure of 26S proteasome.•Fraction of the α5(zeta) subunit undergoes partial proteolysis late in infection.