Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.657135
Title: The synthesis of novel homogeneous glycoproteins
Author: Macmillan, Derek
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 1999
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Abstract:
A glycoprotein can exist as a spectrum of glycosylated forms, where each protein molecule may be associated with an array of oligosaccharide structures. The overall range of glycoforms can have a variety of different biophysical and biochemical properties. As a result of this 'microheterogeneity' there is a need for the synthesis of homogeneously glycosylated proteins for analytical purposes. The synthesis of novel glycoproteins through the selective reaction of glycosyl iodoacetamides with the thiol groups of cysteine has been developed (Figure 10919). Through site-directed mutagenesis, whereby the natural asparagine glycosylation sites can be exchanged for cysteine, it was possible to selectively glycosylated proteins at predetermined sites. This provided a general method for the synthesis of homogeneously glycosylated proteins. We chose the glycoprotein hormone erythropoietin as a model system since the N-glycans at residues 24, 38 and 83 are essential for in vivo biological activity. Using a modified recombinant erythropoietin gene (prepared in Chapter 2) we optimized protein expression, and over-expressed and purified His10-WThEPO, His10-Asn24Cys, His10-Asn38Cys, His10-Asn83Cys and His10-Asn38/83 CyshEPO's in yields of 13mgL-1 from E. coli. This allowed us to probe the structure of rhEPO using techniques such as NMR spectroscopy and electrospray MS (Chapter 3). Having access to larger quantities of EPO, we were also able to develop on-line LC-ESI-MS methods, which allowed us to monitor protein glycosylation reactions with glycosyl β-N-iodoacetamides and map the position of the glycosylation site. The synthesis of relevant iodoacetamides was attempted and simple glycosyl iodoacetamides and 13C labeled iodoacetamides were prepared and successfully employed as probes for protein glycosylation.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.657135  DOI: Not available
Share: