Proteomic Landscape of Adeno-Associated Virus (AAV)-Producing HEK293 Cells

被引:23
|
作者
Strasser, Lisa [1 ]
Boi, Stefano [1 ]
Guapo, Felipe [1 ]
Donohue, Nicholas [1 ]
Barron, Niall [1 ,2 ]
Rainbow-Fletcher, Alana [3 ]
Bones, Jonathan [1 ,2 ]
机构
[1] NIBRT Natl Inst Bioproc Res & Training, Foster Ave, Dublin A94 X099, Ireland
[2] Univ Coll Dublin, Sch Chem & Bioproc Engn, Dublin D04 V1W8, Ireland
[3] Pharmaron, 12 Estuary Banks, Liverpool L24 8RB, Merseyside, England
关键词
proteomics; LC-MS/MS; SP3; label-free quantitation; HEK293; cells; adeno-associated virus (AAV); gene therapy; PLATFORM; DESIGN; VECTOR;
D O I
10.3390/ijms222111499
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adeno-associated viral (AAV) vectors are widely used for gene therapy, providing treatment for diseases caused by absent or defective genes. Despite the success of gene therapy, AAV manufacturing is still challenging, with production yields being limited. With increased patient demand, improvements in host cell productivity through various engineering strategies will be necessary. Here, we study the host cell proteome of AAV5-producing HEK293 cells using reversed phase nano-liquid chromatography and tandem mass spectrometry (RPLC-MS/MS). Relative label-free quantitation (LFQ) was performed, allowing a comparison of transfected vs. untransfected cells. Gene ontology enrichment and pathway analysis revealed differential expression of proteins involved in fundamental cellular processes such as metabolism, proliferation, and cell death. Furthermore, changes in expression of proteins involved in endocytosis and lysosomal degradation were observed. Our data provides highly valuable insights into cellular mechanisms involved during recombinant AAV production by HEK293 cells, thus potentially enabling further improvements of gene therapy product manufacturing.
引用
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页数:14
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