Journal
CHEMICAL COMMUNICATIONS
Volume 58, Issue 67, Pages 9401-9404Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cc02515a
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Funding
- EPSRC
- Cambridge Trusts
- Trinity College Cambridge
- Carlsberg Foundation
- CRUK
- UKRI grants
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In this study, a methodology for the dual-functionalisation of IgG antibodies is developed using disulfide rebridging divinylpyrimidine technology combined with bicyclononyne and methylcyclopropene handles for sequential SPAAC and IEDDA reactions. This strategy is advantageous as it does not require metal catalysis and avoids the need for purification between functionalisation steps.
Herein we report the development of a methodology for the dual-functionalisation of IgG antibodies. This is accomplished through the combination of disulfide rebridging divinylpyrimidine technology, with bicyclononyne and methylcyclopropene handles to facilitate sequential SPAAC and IEDDA reactions. Advantageously, the strategy does not require metal catalysis and avoids the need for purification between functionalisation steps.
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