| AVS 57th International Symposium & Exhibition | |
| Biomaterial Interfaces | Tuesday Sessions |
| Session BI2+AS-TuA |
| Session: | Combining Techniques for Biointerface Characterization |
| Presenter: | M. Dubey, Los Alamos National Laboratory |
| Authors: | M. Dubey, Los Alamos National Laboratory F. Liu, University of Utah H. Takahashi, University of Utah D.W. Grainger, University of Utah D.G. Castner, University of Washington |
| Correspondent: | Click to Email |
This study assesses the capability of high-resolution surface analytical tools to distinguish immobilized antibody orientations on patterned surfaces designed for antibody affinity capture. High-fidelity, side-by-side co-patterning of protein A (antibody Fc domain affinity reagent) and fluorescein (antibody Fab domain hapten) was achieved photo-lithographically on commercial amine-reactive hydrogel polymer surfaces. This was verified from fluorescence imaging using fluorescently labeled protein A and intrinsic fluorescence from fluorescein. Subsequently, dye-labeled murine anti-fluorescein antibody (4-4-20), and antibody Fab and Fc fragments were immobilized from solution onto respective protein A- and fluorescein- co-patterned or control surfaces using antibody-ligand affinity interactions. Fluorescence assays support specific immobilization to fluorescein hapten- and protein A-patterned regions through antigen-antibody recognition and natural protein A-Fc domain interactions, respectively. Affinity-based antibody immobilization on the two different co-patterned surfaces generated side-by-side full antibody “heads-up” and “tails-up” oriented surface patterns. Time-of-flight secondary ion mass spectrometry (ToF-SIMS) analysis, sensitive to chemical information from the top 2-3 nm of the surface, provided ion-specific images of these antibody patterned regions, imaging and distinguishing characteristic ions from amino acids enriched in Fab domains for antibodies oriented in “heads-up” regions, and ions from amino acids enriched in Fc domains for antibodies oriented in “tails-up” regions. Principal component analysis (PCA) improved the distinct ToF-SIMS amino acid compositional and ion-specific surface mapping sensitivity for each “heads-up” versus “tails-up” patterned region. Characteristic Fab and Fc fragment immobilized patterns served as controls. This provides first demonstration of pattern-specific, antibody orientation-dependent surface maps based on antibody domain- and structure- specific compositional differences by ToF-SIMS analysis. Since antibody immobilization and orientation are critical to many technologies, orientation characterization using ToF-SIMS could be very useful and convenient for immobilization quality control and understanding methods for improving the performance of antibody-based surface capture assays.