(349e) AWARD Session: Emergent Properties of Nanosensor Arrays: Applications to Monitoring IgG Affinity Distributions, Weakly-Affined Hypermannosylation, and Colony Selection for Biomanufacturing
It is widely recognized that an array of addressable sensors can be multiplexed for the label-free detection of a library of analytes. However, such arrays have useful properties that emerge from the ensemble, even when monofunctionalized. As examples, we show that an array of nanosensors can estimate the mean and variance of the observed dissociation constant (KD), using three different examples of binding IgG with Protein-A as the recognition site, including polyclonal human IgG (KD µ = 19 µM, σ2 = 1000 mM2), murine IgG (KD µ = 4.3 nM, σ2 = 3 µM2), and human IgG from CHO cells (KD µ = 2.5 nM, σ2 = 0.01 µM2). Second, we show that an array of nanosensors can uniquely monitor weakly-affined analyte interactions via the increased number of observed interactions. One application involves monitoring the metabolically-induced hypermannosylation of human IgG from CHO using PSA-lectin conjugated sensor arrays where temporal glycosylation patterns are measured and compared. Lastly, the array of sensors can also spatially map the local production of an analyte from cellular biosynthesis, thus providing a powerful approach to clonal selection. As an example, we rank productivity of IgG-producing HEK colonies cultured directly on the array of nanosensors itself. This study opens new avenues for the use of nanosensor arrays for biomanufacturing applications.