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Title: Using data to characterise the relationship between nanobody sequence, structure and function
Author: Mitchell, Laura Sophie
ISNI:       0000 0004 7968 4897
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 2019
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Nanobodies (Nbs) are a class of single-domain antibody derived from the immune systems of camelid species. They achieve binding affinities and specificities to target antigens comparable to those of classical antibodies (Abs), despite being ten times smaller (~15 kDa) and having only three variable loops. This raises the question of how these binding affinities and specificities are achieved in such a compact molecule. To address this, a novel dataset of Nb-antigen co-crystal structures are assembled and investigated. Findings are presented in three main chapters, with a fourth describing a collaborative Nb engineering project. First, the sequence and structural diversity of Nb domains is analysed and compared with that observed in a comparative set of Ab domains. Nbs are shown to display greater structural diversity across all three loops, in conjunction with enhanced conservation across the framework regions. Second, the way in which Nbs bind antigens is investigated. Class-averaged properties of antigen-contacting residues (the `paratope'), show Nb paratopes are more variable than those of Abs. This is true for both the distribution of paratope residues across the domain, and the types of residues used at interfaces. Notably, Nbs deviate from the `loops = paratope' assumption which is true for Abs; an insight which has implications for Nb selection, modelling and engineering strategies. Third, the sequence-structure-paratope relationship of Nb CDR H3 loops is interrogated. Previous chapters show the H3 loop is the most structurally diverse region, and critical in determining antigen-binding specificity. Here, Nbs are clustered into three distinct classes based on H3 loop structural features. The classes have distinct sequence features and use different distributions of paratope residues; suggesting loop conformation and antigen-binding orientation may be inferred from Nb sequence. Finally, an anti-GFP Nb is engineered by structure-guided mutagenesis for enhanced binding to a closely related antigen. The engineered Nb is being trialled for use in a novel super resolution microscopy method.
Supervisor: Colwell, Lucy Jane Sponsor: BBSRC
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
Keywords: nanobody ; antibody ; nb ; paratope ; vhh ; vh