Research
Epitranscriptomics & Cancer Adaptation : A.David

Activities

Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

More..

Zotero public

Added by mollevi
Last modified by alainmange
Group name PlateformePP2I
Item Type Journal Article
Title A method to confer Protein L binding ability to any antibody fragment
Creator Lakhrif et al.
Author Zineb Lakhrif
Author Martine Pugnière
Author Corinne Henriquet
Author Anne di Tommaso
Author Isabelle Dimier-Poisson
Author Philippe Billiald
Author Matthieu O. Juste
Author Nicolas Aubrey
Abstract Recombinant antibody single-chain variable fragments (scFv) are difficult to purify homogeneously from a protein complex mixture. The most effective, specific and fastest method of purification is an affinity chromatography on Protein L (PpL) matrix. This protein is a multi-domain bacterial surface protein that is able to interact with conformational patterns on kappa light chains. It mainly recognizes amino acid residues located at the VL FR1 and some residues in the variable and constant (CL) domain. Not all kappa chains are recognized, however, and the lack of CL can reduce the interaction. From a scFv composed of IGKV10-94 according to IMGT®, it is possible, with several mutations, to transfer the motif from the IGKV12-46 naturally recognized by the PpL, and, with the single mutation T8P, to confer PpL recognition with a higher affinity. A second mutation S24R greatly improves the affinity, in particular by modifying the dissociation rate (kd). The equilibrium dissociation constant (KD) was measured at 7.2 10(-11) M by surface plasmon resonance. It was possible to confer PpL recognition to all kappa chains. This protein interaction can be modulated according to the characteristics of scFv (e.g., stability) and their use with conjugated PpL. This work could be extrapolated to recombinant monoclonal antibodies, and offers an alternative for protein A purification and detection.
Publication mAbs
Volume 8
Issue 2
Pages 379-388
Date 2016
Journal Abbr MAbs
Language eng
DOI 10.1080/19420862.2015.1116657
ISSN 1942-0870
Library Catalog PubMed
Extra PMID: 26683650 PMCID: PMC4966575
Tags Amino Acid Motifs, antibody, Atffinity, author, Bacterial Proteins, Chromatography, Affinity, detection, Fab, Humans, Immunoglobulin kappa-Chains, Mutation, Missense, original, pp2i, protein L (PpL), purification, Recombinant Fusion Proteins, scFv, Single-Chain Antibodies
Date Added 2019/06/04 - 17:32:17
Date Modified 2020/01/14 - 10:26:13


© Institut de Recherche en Cancérologie de Montpellier - 2011 - Tous droits réservés - Mentions légales - Connexion - Conception : ID Alizés