A set of 70 variable domains of heavy chain Camelid antibodies (VHHs) were grown under identical conditions in yeast. The production yields in Saccharomyces cerevisiae ranged between nearly 0 and 150 mg/l. To understand these large differences in production of VHHs, even those recognizing the same antigen or those with a high sequence similarity, we searched for correlations between a series of aspects of the sequences and features of 3D structures and the production yield. Several parameters on DNA sequence and protein sequence level were analysed using simple bioinformatics techniques. No trivial correlations were found. We did notice many non-optimal codons. Visual inspection of the multiple sequence alignment revealed an enrichment of c...
The goal of this research is to understand how three different parameters affect single chain variab...
Species of the Camelidae family possess a class of antibodies consisting only of heavy chains. The v...
Antigen recognition by mammalian antibodies represents the most diverse setting for protein-protein ...
Variable domains of camelid heavy chain antibodies (VHHs) are the smallest available antigen binding...
Variable domains of camelid heavy chain antibodies (VHHs) are the smallest available antigen binding...
Item does not contain fulltextVariable domains of llama heavy-chain antibodies (VHH) are becoming a ...
International audienceBackground: A large fraction of camelid (camels and llamas) antibodies is comp...
International audienceAntigen binding by antibodies requires precise orientation of the complementar...
International audienceTherapeutic antibodies have transformed the clinical practice. Not surprisingl...
Microbicides offer a promising way to prevent HIV infection in developing countries. Llama heavy cha...
The aim of this study was to improve production level of llama heavy chain antibody fragments (V (HH...
The work presented in this thesis focusses on the sequence and structural analysis of antibodies and...
The capturing of antibodies and their variant formats by Staphylococcal protein A (SpA; Protein-A) h...
<p>(A) Sequence alignment of unique single domain VHH antibodies specific to pandemic H1N1 isolated ...
<div><p>Antibody development is still associated with substantial risks and difficulties as single m...
The goal of this research is to understand how three different parameters affect single chain variab...
Species of the Camelidae family possess a class of antibodies consisting only of heavy chains. The v...
Antigen recognition by mammalian antibodies represents the most diverse setting for protein-protein ...
Variable domains of camelid heavy chain antibodies (VHHs) are the smallest available antigen binding...
Variable domains of camelid heavy chain antibodies (VHHs) are the smallest available antigen binding...
Item does not contain fulltextVariable domains of llama heavy-chain antibodies (VHH) are becoming a ...
International audienceBackground: A large fraction of camelid (camels and llamas) antibodies is comp...
International audienceAntigen binding by antibodies requires precise orientation of the complementar...
International audienceTherapeutic antibodies have transformed the clinical practice. Not surprisingl...
Microbicides offer a promising way to prevent HIV infection in developing countries. Llama heavy cha...
The aim of this study was to improve production level of llama heavy chain antibody fragments (V (HH...
The work presented in this thesis focusses on the sequence and structural analysis of antibodies and...
The capturing of antibodies and their variant formats by Staphylococcal protein A (SpA; Protein-A) h...
<p>(A) Sequence alignment of unique single domain VHH antibodies specific to pandemic H1N1 isolated ...
<div><p>Antibody development is still associated with substantial risks and difficulties as single m...
The goal of this research is to understand how three different parameters affect single chain variab...
Species of the Camelidae family possess a class of antibodies consisting only of heavy chains. The v...
Antigen recognition by mammalian antibodies represents the most diverse setting for protein-protein ...