The insect cell-baculovirus expression vector (BEV) system is widely used to produce recombinant proteins and has greatly facilitated basic biomedical research on protein structure, function, and the roles of various proteins in disease. This system also is used to produce recombinant proteins for direct biomedical applications. The use of this system, which will have a profound impact on medicine, ultimately depends upon a clear understanding of protein biosynthesis and processing pathways in insect cells. However, because insect cell protein processing pathways are not a major subject of basic research, important questions remain to be resolved. This proposal focuses on one of these questions: What is the nature of the N-glycosylation pathway in insect cells? Our current view of this pathway is confused and it is difficult to predict what kind of glycan one will find on a recombinant glycoprotein produced in the insect cell-BEV system. We have developed a working model of the insect cell N-glycosylating pathway and the overall goal of this proposal is to evaluate and extend this model.
The specific aims are: (1) to introduce additional mammalian processing enzymes into insect cells and determine how this affects their N-glycosylation pathway; (2) to evaluate the capabilities and biomedical applications of insect cell-BEV expression systems with genetically engineered N-glycosylation pathways; (3) to isolate and characterize new insect cell genes encoding glycoprotein processing enzymes; (4) to examine the cell biology and biochemistry of insect cell glycoprotein processing enzymes; (5) to examine the effects of baculovirus infection on the insect cell secretory pathway; and, (6) to determine if insects have beta1, 4-galactosyltransferase. This work has practical value and could yield improved systems for the production of therapeutic glycoproteins or for liver-biosynthetic pathway that clearly differs from the corresponding pathway in higher eucaryotes. A better understanding of the insect cell pathway might help us to understand how protein glycosylation pathways evolved and how carbohydrate processing impacts glycoprotein function. Furthermore, well-defined differences in insect protein glycosylation pathways might be exploited as specific targets for novel pesticide development in the future. This could lead to more effective ways to control medically and agriculturally significant insects and/or the diseases they help to spread, which would have a major impact on worldwide public health.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM049734-06
Application #
6018961
Study Section
Special Emphasis Panel (ZRG5-TMP (01))
Project Start
1994-08-01
Project End
2002-07-31
Budget Start
1999-08-01
Budget End
2000-07-31
Support Year
6
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Wyoming
Department
Biochemistry
Type
Schools of Earth Sciences/Natur
DUNS #
069690956
City
Laramie
State
WY
Country
United States
Zip Code
82071
Harrison, Robert L; Jarvis, Donald L (2016) Transforming Lepidopteran Insect Cells for Continuous Recombinant Protein Expression. Methods Mol Biol 1350:329-48
Serena, María Soledad; Geisler, Christoph; Metz, Germán Ernesto et al. (2016) Production of pseudorabies virus recombinant glycoprotein B and its use in an agar gel immunodiffusion (AGID) test for detection of antibodies with sensitivity and specificity equal to the virus neutralization assay. J Virol Methods 230:9-12
Harrison, Robert L; Jarvis, Donald L (2016) Transforming Lepidopteran Insect Cells for Improved Protein Processing and Expression. Methods Mol Biol 1350:359-79
Mabashi-Asazuma, Hideaki; Sohn, Bong-Hee; Kim, Young-Soo et al. (2015) Targeted glycoengineering extends the protein N-glycosylation pathway in the silkworm silk gland. Insect Biochem Mol Biol 65:20-7
Geisler, Christoph; Mabashi-Asazuma, Hideaki; Kuo, Chu-Wei et al. (2015) Engineering ?1,4-galactosyltransferase I to reduce secretion and enhance N-glycan elongation in insect cells. J Biotechnol 193:52-65
Toth, Ann M; Kuo, Chu-Wei; Khoo, Kay-Hooi et al. (2014) A new insect cell glycoengineering approach provides baculovirus-inducible glycogene expression and increases human-type glycosylation efficiency. J Biotechnol 182-183:19-29
Mabashi-Asazuma, Hideaki; Kuo, Chu-Wei; Khoo, Kay-Hooi et al. (2014) A novel baculovirus vector for the production of nonfucosylated recombinant glycoproteins in insect cells. Glycobiology 24:325-40
Lin, Chi-Hung; Kuo, Chu-Wei; Jarvis, Donald L et al. (2014) Facile removal of high mannose structures prior to extracting complex type N-glycans from de-N-glycosylated peptides retained by C18 solid phase to allow more efficient glycomic mapping. Proteomics 14:87-92
Serena, María Soledad; Geisler, Christoph; Metz, Germán Ernesto et al. (2013) Expression and purification of Suid Herpesvirus-1 glycoprotein E in the baculovirus system and its use to diagnose Aujeszky's disease in infected pigs. Protein Expr Purif 90:1-8
Lin, Chi-Hung; Jarvis, Donald L (2013) Utility of temporally distinct baculovirus promoters for constitutive and baculovirus-inducible transgene expression in transformed insect cells. J Biotechnol 165:11-7

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