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Polarization-Multiplexed Bloch Surface Wave Sensing of Single-Strand DNA Growth
Jonathan Barolak1, Erika Mogni1, Giovanni Pellegrini2
1Dipartimento di Fisica, Politecnico di Milano, 20133Milano, Italy.
Abstract:
Refractometric biosensing is a vital label-free tool for the real-time detection and interaction analysis of biological and chemical substances. Nanophotonic platforms like surface plasmon resonance (SPR) have played a critical role in providing refractometric sensing capabilities for clinical diagnostics and environmental monitoring. However, traditional systems operating in a single-polarization state cannot fully characterize optical properties such as birefringence, which is crucial to resolve many complex biological interactions. Although Bloch surface wave (BSW) sensors can support both transverse electric (TE) and transverse magnetic (TM) modes, a key capability SPR lacks, they have historically been implemented in single-mode configurations. In this paper, we present a polarization-multiplexed BSW refractometric sensing system, simultaneously tracking the resonant wavelength shifts of both TE and TM BSW modes through time. Our technique was applied to investigate single-strand DNA growth during rolling circle amplification (RCA). To accurately recover the time-dependent birefringence, capturing dynamics of the DNA growth and orientation of its chains, we implemented a two-stage modeling approach based on the transfer matrix method (TMM). First, we utilized a wavelength-dependent surface sensitivity model, confining refractive index changes to the immediate layer above the crystal, to distinguish isotropic background dynamics from birefringent signals. Following the onset of RCA, we transitioned to a model that accounted for the vertical growth of the DNA layers in time. By fitting this model to the TE and TM resonant shifts, we monitor the growth rate of the single-strand DNA layer, as well as the refractive index along the two polarization components. Our findings demonstrate the platform's ability to resolve the structural evolution of complex biomolecular interactions associated with conformational changes.