Consecutive Mechano-Immunophenotyping of Single Cells in a Photopatterned Microfluidic Channel

在光刻图案化微流控通道中对单个细胞进行连续力学-免疫表型分析

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Abstract

Physical forces act on cells alongside biochemical signals, yet single-cell assays rarely capture both dimensions simultaneously. We present a two-stage microfluidic device that extracts mechanical and molecular phenotypes in one pass. As cells squeeze through dual 6 μm constrictions, their deformability appears as transit time T (D) . Immediately downstream, a 350 μm-long hydrogel photopatterned microchannel with antibody transiently captures cells proportionally to the cell surface-antigen density, yielding an additional delay T (A) . Using biotinylated anti-CD64 and anti-CD44v9, we profiled five cancer cell lines and uncovered a mechanical-immunochemical correlation up to R (2) = 0.41 for HeLa cells and high heterogeneity for HT29 cells. The platform interrogates ∼100 cells min(-1), detects ∼100 membrane proteins μm(-2), and preserves viability for downstream culture or genome sequencing. Because the hydrogel can host multiple ligands, the method enables multiplex, mechanomolecular phenotyping for precision oncology, stem-cell quality control, and mechanotargeted drug screening.

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