Characterization of Phosphorylation-Dependent Antibody Binding to Cancer-Mutated Linkers of C 2 H 2 Zinc Finger Proteins by Intact Transition Epitope Mapping-Thermodynamic Weak-Force Order Analysis

• Published in: Journal of the American Society for Mass Spectrometry Vol. 34; no. 2; pp. 171 - 181
• Main Authors: Scherf, Maximilian, Koy, Cornelia, Röwer, Claudia, Neamtu, Andrei, Glocker, Michael O
• Format: Journal Article
• Language: English
• Published: United States 01.02.2023
• Subjects: Amino Acids; Antigen-Antibody Complex; Epitope Mapping - methods; Humans; Ions; Neoplasms; Peptides - chemistry; Phosphorylation; Zinc Fingers; ITEM-TWO; antibody; immune complex; zinc finger protein; mass spectrometry; cancer-related mutation; nanoESI-MS
• ISSN: 1044-0305; 1879-1123
• DOI: 10.1021/jasms.2c00244

With Intact Transition Epitope Mapping-Thermodynamic Weak-force Order (ITEM-TWO) analysis in combination with molecular modeling, the phosphorylation-dependent molecular recognition motif of the anti-HpTGEKP antibody has been investigated with binary and ternary component mixtures consisting of antibody and (phospho-) peptides. Amino acid sequences have been selected to match either the antibody's recognition motif or the cancer-related zinc finger protein mutations and phosphorylations of the respective amino acid residues. Upon electrospraying of all the components of the mixtures, that is, hexapeptides, antibody, and intact immune complexes, the produced ions were subjected to mass spectrometric mass filtering. The antibody ions as well as the immune complex ions traversed into the mass spectrometer's collision chamber, whereas paths of unbound peptide ions were blocked prior to entering the collision cell. After dissociation of the multiply charged immune complexes in the gas phase, the complex-released peptide ions were recorded after having traversed the second mass filter. Complex-released peptides were unambiguously identified by their masses using mass analysis with isotope resolution. From the results of our studies with seven (phospho-) peptides with distinct amino acid sequences, which resembled either the antibody's binding motif or mutations, we conclude the following: (i) A negatively charged phospho group, located near the peptide's N-terminus is mandatory for antibody binding when placed on the peptide surface at a precise distance to the C-terminally located positively charged ε-amino group of a lysinyl residue. (ii) A bulky amino acid residue, such as the tyrosinyl residue at the N-terminal position of the (phospho-) threoninyl residue, abolishes antibody binding. (iii) Two closely spaced phospho groups negatively interfere with the surface polarity pattern and abolish antibody binding as well. (iv) Non-phosphorylated peptides are not binding partners of the anti-HpTGEKP antibody.