Antigen binding forces of individually addressed single-chain Fv antibody molecules
Author(s) -
Robert Ros,
Falk Schwesinger,
Dario Anselmetti,
Martina Kubon,
Rolf Schäfer,
Andreas Plückthun,
Louis Tiefenauer
Publication year - 1998
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.95.13.7402
Subject(s) - chemistry , molecule , covalent bond , ligand (biochemistry) , antigen , biophysics , molecular binding , atomic force microscopy , nanotechnology , biochemistry , materials science , biology , receptor , genetics , organic chemistry
Antibody single-chain Fv fragment (scFv) molecules that are specific for fluorescein have been engineered with a C-terminal cysteine for a directed immobilization on a flat gold surface. Individual scFv molecules can be identified by atomic force microscopy. For selected molecules the antigen binding forces are then determined by using a tip modified with covalently immobilized antigen. An scFv mutant of 12% lower free energy for ligand binding exhibits a statistically significant 20% lower binding force. This strategy of covalent immobilization and measuring well separated single molecules allows the characterization of ligand binding forces in molecular repertoires at the single molecule level and will provide a deeper insight into biorecognition processes.
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