Hybrid Supercharged Antibodies: A Rational Approach to Boost Immunoassay Sensitivity via Controlled Nanoparticle Adsorption
This study presents a novel approach to enhance the sensitivity of a lateral flow immunoassay by computationally designing supercharged antibodies that optimize both the adsorption amount and molecular orientation on nanoparticle surfaces. We engineered immunoglobulin G antibodies with positively charged Fc domains and negatively charged Fab domains to create charge-polarized molecules for controlled interaction with negatively charged cellulose nanoparticles (NanoAct). The supercharged antibodies retained physicochemical properties and antigen-binding affinities identical to those of the wild-type antibody. Quantitative analysis showed that positively supercharged Fc domains enhanced antibody adsorption, and the charge-polarized design (featuring a negatively charged Fab and a positively charged Fc; c-10/Fc-pos14) enhanced relative Fab accessibility on the nanoparticle surface. Interaction analyses between supercharged antibodies and NanoAct using isothermal titration calorimetry quantitatively revealed that the c-10/Fc-pos14 antibody adsorbed onto NanoAct in the tail-on orientation. Consequently, lateral flow immunoassay performance tests demonstrated an 8-fold improvement in the limit of detection from 25 to 3.13 ng/mL, without increasing nonspecific binding. The key design principle involves maintaining sufficient charge separation between the domains to ensure proper orientation control. This supercharging approach represents a promising strategy for boosting immunoassay sensitivity while preserving sufficiently low noise levels with potential applications in other antibody-based diagnostic platforms.
Authors
- José M. M. Caaveiro (ORCID: https://orcid.org/0000-0001-5568-2369)
- Satoru Nagatoishi (ORCID: https://orcid.org/0000-0002-0794-3963)
- Keisuke Murakami (ORCID: https://orcid.org/0000-0001-5297-055X)
- Hirokazu Nagai
- K. Kasahara
- Junichi Sato
- Daisuke Kuroda
- Kouhei Tsumoto
Institutions
- Nihon University (JP)
- Kyushu University (JP)
- Asahi Kasei (Japan) (JP)
- Mitsui (Japan) (JP)
- The University of Tokyo (JP)
Publication Details
- Journal
- Langmuir
- Published
- 2026-04-03
- DOI
- https://doi.org/10.1021/acs.langmuir.5c06029
- Primary Topic
- Monoclonal and Polyclonal Antibodies Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Agency for Medical Research and Development
- Ministry of Education, Culture, Sports, Science and Technology
- University of Tokyo
- National Institutes of Health
- University of California, San Francisco
- Japan Society for the Promotion of Science
- Institute of Medical Science, University of Tokyo