Literature DB >> 31683061

Intact Transition Epitope Mapping - Thermodynamic Weak-force Order (ITEM - TWO).

Bright D Danquah1, Yelena Yefremova1, Kwabena F M Opuni2, Claudia Röwer1, Cornelia Koy1, Michael O Glocker3.   

Abstract

We have developed an electrospray mass spectrometry method which is capable to determine antibody affinity in a gas phase experiment. A solution with the immune complex is electrosprayed and multiply charged ions are translated into the gas phase. Then, the intact immune-complex ions are separated from unbound peptide ions. Increasing the voltage difference in a collision cell results in collision induced dissociation of the immune-complex by which bound peptide ions are released. When analyzing a peptide mixture, measuring the mass of the complex-released peptide ions identifies which of the peptides contains the epitope. A step-wise increase in the collision cell voltage difference changes the intensity ratios of the surviving immune complex ions, the released peptide ions, and the antibody ions. From all the ions´ normalized intensity ratios are deduced the thermodynamic quasi equilibrium dissociation constants (KDm0g#) from which are calculated the apparent gas phase Gibbs energies of activation over temperature (ΔGm0g#T). The order of the apparent gas phase dissociation constants of four antibody - epitope peptide pairs matched well with those obtained from in-solution measurements. The determined gas phase values for antibody affinities are independent from the source of the investigated peptides and from the applied instrument. Data are available via ProteomeXchange with identifier PXD016024. SIGNIFICANCE: ITEM - TWO enables rapid epitope mapping and determination of apparent dissociation energies of immune complexes with minimal in-solution handling. Mixing of antibody and antigen peptide solutions initiates immune complex formation in solution. Epitope binding strengths are determined in the gas phase after electrospraying the antibody / antigen peptide mixtures and mass spectrometric analysis of immune complexes under different collision induced dissociation conditions. Since the order of binding strengths in the gas phase is the same as that in solution, ITEM - TWO characterizes two most important antibody properties, specificity and affinity.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Antibody affinity determination; Antibody specificity determination; Mass spectrometric epitope mapping; Nano-electrospray mass spectrometry; Native MS; Q-ToF analyzer

Mesh:

Substances:

Year:  2019        PMID: 31683061     DOI: 10.1016/j.jprot.2019.103572

Source DB:  PubMed          Journal:  J Proteomics        ISSN: 1874-3919            Impact factor:   4.044


  2 in total

1.  ITEM-THREE analysis of a monoclonal anti-malaria antibody reveals its assembled epitope on the pfMSP119 antigen.

Authors:  Kwabena F M Opuni; Cornelia Koy; Manuela Russ; Maren Reepmeyer; Bright D Danquah; Moritz Weresow; Astrid Alef; Peter Lorenz; Hans-Juergen Thiesen; Michael O Glocker
Journal:  J Biol Chem       Date:  2020-08-26       Impact factor: 5.157

2.  Mass Spectrometric Analysis of Antibody-Epitope Peptide Complex Dissociation: Theoretical Concept and Practical Procedure of Binding Strength Characterization.

Authors:  Bright D Danquah; Kwabena F M Opuni; Claudia Roewer; Cornelia Koy; Michael O Glocker
Journal:  Molecules       Date:  2020-10-17       Impact factor: 4.411

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.