Antibodies are a hallmark in Multiple Sclerosis (MS), and a group of them can be measured using CSF114(Glc), a synthetic peptide bearing an N-glucosyl group on Asn side chain, possibly because the peptide reproduces aberrant post-translational glycosylations on myelin proteins as target of autoantibodies [1]. It has already been demonstrated that in vitro panning procedures allow to obtain structure sensitive antibody fragments [2], and it is widely accepted that a single variable heavy (VH) domain isolated from natural antibodies may contribute to antigen binding with comparable affinities and specificities to whole antibody [3,4]. We reasoned that antibodies raised against this probe could have been relevant for MS. The aim of this work was the isolation of a panel of soluble hVH antibody fragments against the glucopeptide CSF114(Glc) from a synthetic human domain antibody library [5].
Surface Plasmon Resonance to Select and Characterize Recombinant Human Domain Antibodies / F. Real-Fernández, G. Rossi, F. Niccheri, M. Ramazzotti, D. Degl'Innocenti, F. Lolli, A.M. Papini, P. Rovero. - ELETTRONICO. - (2014), pp. 268-269.
Surface Plasmon Resonance to Select and Characterize Recombinant Human Domain Antibodies.
F. Real-Fernández;G. Rossi;F. Niccheri;M. Ramazzotti;D. Degl'Innocenti;F. Lolli;A. M. Papini;P. Rovero
2014
Abstract
Antibodies are a hallmark in Multiple Sclerosis (MS), and a group of them can be measured using CSF114(Glc), a synthetic peptide bearing an N-glucosyl group on Asn side chain, possibly because the peptide reproduces aberrant post-translational glycosylations on myelin proteins as target of autoantibodies [1]. It has already been demonstrated that in vitro panning procedures allow to obtain structure sensitive antibody fragments [2], and it is widely accepted that a single variable heavy (VH) domain isolated from natural antibodies may contribute to antigen binding with comparable affinities and specificities to whole antibody [3,4]. We reasoned that antibodies raised against this probe could have been relevant for MS. The aim of this work was the isolation of a panel of soluble hVH antibody fragments against the glucopeptide CSF114(Glc) from a synthetic human domain antibody library [5].I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.