: Antibody single-chain Fv (scFv) fragments are able to form dimers under certain conditions, and the extent of dimerization appears to depend on linker length, antibody sequence, and external factors. We analyzed the factors influencing dimer-monomer equilibrium as well as the rate of interconversion, using the scFv McPC603 as a model system. In this molecule, the stability of the VH-VL interaction can be conveniently varied by adjusting the ionic strength (because of its influence on the hydrophobic effect), by pH (presumably because of the presence of titratable groups in the interface), and by the presence or absence of the antigen phosphorylcholine, which can be rapidly removed due to its very fast off-rate. It was found that th...
The spontaneous formation of aggregates presents an obstacle in the developability, manufacturabilit...
AbstractThe structure of the Fab fragment of the monoclonal antibody MAK 33 (κ/IgG1) at pH 2 was cha...
International audienceWe have analyzed conformational changes that occur at the interface between th...
AbstractBy varying linker length and domain orientation three multivalent derivatives of a monovalen...
Intermolecular interactions and conformation in dimer species of Palivizumab, a monoclonal antibody ...
By constructing Fv and single-chain Fv (scFv) fragments of antibodies, the variable domains are take...
Background: Antibodies are prototypes of multimeric proteins and consist of structurally similar dom...
AbstractThe equilibrium denaturation and unfolding kinetics of the domains VL and VH have been compa...
Depending on the linker length between the VH and the VL domain, single-chain Fv (scFv) antibody fra...
2To whom correspondence should be addressed A systematic study has been performed on the relationshi...
The folding and assembly of the Fv fragment of the phosphorylcholine binding antibody McPC603, a non...
Robinson, Anne S.The focus of this thesis is to study the refolding of single-chain antibodies (scFv...
To investigate structure and function of different monoclonal antibody (MAb) dimers.MAb dimers were ...
Antibody variable domains vary widely in their intrinsic thermodynamic stability. Despite the mutual...
The binding of divalent haptens to IgE-class antibodies leads predominantly to their oligomerization...
The spontaneous formation of aggregates presents an obstacle in the developability, manufacturabilit...
AbstractThe structure of the Fab fragment of the monoclonal antibody MAK 33 (κ/IgG1) at pH 2 was cha...
International audienceWe have analyzed conformational changes that occur at the interface between th...
AbstractBy varying linker length and domain orientation three multivalent derivatives of a monovalen...
Intermolecular interactions and conformation in dimer species of Palivizumab, a monoclonal antibody ...
By constructing Fv and single-chain Fv (scFv) fragments of antibodies, the variable domains are take...
Background: Antibodies are prototypes of multimeric proteins and consist of structurally similar dom...
AbstractThe equilibrium denaturation and unfolding kinetics of the domains VL and VH have been compa...
Depending on the linker length between the VH and the VL domain, single-chain Fv (scFv) antibody fra...
2To whom correspondence should be addressed A systematic study has been performed on the relationshi...
The folding and assembly of the Fv fragment of the phosphorylcholine binding antibody McPC603, a non...
Robinson, Anne S.The focus of this thesis is to study the refolding of single-chain antibodies (scFv...
To investigate structure and function of different monoclonal antibody (MAb) dimers.MAb dimers were ...
Antibody variable domains vary widely in their intrinsic thermodynamic stability. Despite the mutual...
The binding of divalent haptens to IgE-class antibodies leads predominantly to their oligomerization...
The spontaneous formation of aggregates presents an obstacle in the developability, manufacturabilit...
AbstractThe structure of the Fab fragment of the monoclonal antibody MAK 33 (κ/IgG1) at pH 2 was cha...
International audienceWe have analyzed conformational changes that occur at the interface between th...