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Sanjuan Nandin et al. describe an innovative approach based on antigen-dependent activation of human memory B cells in culture. It results in the rapid generation of human antibodies against infectious agents and offers the potential for therapeutic antibody production and vaccine development., Vaccines remain the most effective tool to prevent infectious diseases. Here, we introduce an in vitro booster vaccination approach that relies on antigen-dependent activation of human memory B cells in culture. This stimulation induces antigen-specific B cell proliferation, differentiation of B cells into plasma cells, and robust antibody secretion after a few days of culture. We validated this strategy using cells from healthy donors to retrieve human antibodies against tetanus toxoid and influenza hemagglutinin (HA) from H1N1 and newly emergent subtypes such as H5N1 and H7N9. Anti-HA antibodies were cross-reactive against multiple subtypes, and some showed neutralizing activity. Although these antibodies may have arisen as a result of previous influenza infection, we also obtained gp120-reactive antibodies from non–HIV-infected donors, indicating that we can generate antibodies without prior antigenic exposure. Overall, our novel approach can be used to rapidly produce therapeutic antibodies and has the potential to assess the immunogenicity of candidate antigens, which could be exploited in future vaccine development.

Molecular transport in living systems regulates numerous processes underlying biological function. Although many cellular components exhibit anomalous diffusion, only recently has the subdiffusive motion been associated with nonergodic behavior. These findings have stimulated new questions for their implications in statistical mechanics and cell biology. Is nonergodicity a common strategy shared by living systems? Which physical mechanisms generate it? What are its implications for biological function? Here, we use single particle tracking to demonstrate that the motion of DC-SIGN, a receptor with unique pathogen recognition capabilities, reveals nonergodic subdiffusion on living cell membranes. In contrast to previous studies, this behavior is incompatible with transient immobilization and therefore it can not be interpreted according to continuous time random walk theory. We show that the receptor undergoes changes of diffusivity, consistent with the current view of the cell membrane as a highly dynamic and diverse environment. Simulations based on a model of ordinary random walk in complex media quantitatively reproduce all our observations, pointing toward diffusion heterogeneity as the cause of DC-SIGN behavior. By studying different receptor mutants, we further correlate receptor motion to its molecular structure, thus establishing a strong link between nonergodicity and biological function. These results underscore the role of disorder in cell membranes and its connection with function regulation. Due to its generality, our approach offers a framework to interpret anomalous transport in other complex media where dynamic heterogeneity might play a major role, such as those found, e.g., in soft condensed matter, geology and ecology., 27 pages, 5 figures

Receptor nanoclustering prior to ligand activation is rapidly emerging as an essential feature common to most cell membranes. Yet, the mechanisms governing this distinct spatial patterning and functional role are still poorly understood. We used a combination of biochemical and advanced biophysical techniques, including optical superresolution and single particle tracking, to investigate the spatiotemporal organization of DC-SIGN, a pathogen recognition receptor that homo-oligomerizes in-vitro. We found an intrinsic nanoclustering capacity of DC-SIGN (ca. 180 nm in size) far beyond basal tetramerization, which strictly depended on its molecular structure. DC-SIGN nanoclusters exhibited Brownian diffusion on the cell membrane with values of the order of 10−2 μm2/s. Truncation of the neck region, known to abrogate tetramerization, significantly reduced nanoclustering and concomitantly increased lateral diffusion. Importantly, DC-SIGN nanocluster dissolution compromised DC-SIGN binding to nanoscale size pathogens. As such, our results underscore a direct relationship between spatial nanopatterning, driven by intermolecular interactions between the neck regions, and receptor diffusion to provide DC-SIGN with the exquisite ability to dock pathogens at the virus length-scale. We suggest that protein-protein interactions facilitated by structural molecular motifs might represent a so far underestimated but general mechanism to pre-organize receptors on the cell membrane for efficient action under stimulated conditions.

The application of techniques such as fluorescence correlation spectroscopy and single particle tracking to the plasma membrane of living cells continuously evidences subdiffusive motion of proteins and lipids. This anomalous motion is generally associated to the interplay of molecular crowding, diffusion barriers and specific interactions. Addressing the cause of subdiffusion is essential for understanding molecular mechanisms underlying cellular function, such as target search, kinetics of transport-limited reactions, trafficking and signalling. Recently, the subdiffusive motion of some cellular and membrane components has been associated to weak ergodicity breaking and attributed to transient immobilization caused by interactions with microtubules or actin cytoskeleton. These works have opened new questions about the role of nonergodic subdiffusion in the dynamics of living systems.By means of single particle tracking experiments, we show that the dynamics of DC-SIGN, a transmembrane receptor with unique pathogen recognition capabilities, also reveals subdiffusion with signatures of weak ergodicity breaking and aging. In contrast to other biological systems, we demonstrate that DC-SIGN nonergodic subdiffusion cannot be explained by transient immobilization, but rather is compatible with dynamical heterogeneity induced by spatiotemporal changes of diffusivity. While nonergodic diffusion due to long-lived immobilization events can be understood within the framework of continuous-time random walk, our experimental data are accurately interpreted through a new theoretical model describing anomalous transport in biological systems and complex media. A comprehensive analysis of mutated forms of the receptor allowed us to establish a link between receptor molecular structure, nonergodic diffusion and function. Our results underscore the role of spatiotemporal disorder in the dynamics of cell membrane receptors. In addition, they have broad implications to other heterogeneous systems where the occurrence of nonergodicity remains unexplored.