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Engineering the heavy chain constant region of human IgG to modulate glycosylation and effector functions

ReferenceSBD07526
Principal Investigator / Supervisor Professor R Jefferis
Co-Investigators /
Co-Supervisors
Institution University of Birmingham
DepartmentMedical Sciences - Medicine
Funding typeResearch
Value (£) 233,940
StatusCompleted
TypeResearch Grant
Start date 01/08/1997
End date 01/08/2000
Duration36 months

Abstract

Oligosaccharide homogeneity and consistency poses significant problems for the production of recombinant glycoproteins intended for therapeutic use. We aim to use protein engineering to design antibody constructs that will direct glycosylation towards homogeneity with or without compromised biological activities such as phagocytosis, complement-mediated lysis, or biological half-life. Oligosaccharide structures will be analysed by HPLC and MALDI-TOF mass spectrometry. We will define the minimal structural unit of Fc that will mediate selected effector functions, expressing the CH2 domain in different protein environments, for eventual expression in fusion proteins.

Summary

unavailable
Committee Closed Committee - Biomolecular Sciences (BMS)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative Structural biology and design applications (SBD) [1996]
Funding SchemeX – not Funded via a specific Funding Scheme
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