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Biology subjects

Li, T.-D.

Publications and source records attributed to Li, T.-D..

2 recordsLinked to original sources

Non-invasive Biomechanical Characterization of Embryos Using Microfluidic Cantilevers

Embryonic development is intricately regulated by mechanical properties such as stiffness, which influence developmental viability and implantation success - factors critical in assisted reproductive technologies (ART). Traditional embryo evaluation relies predominantly on morphology, lacking quantitative mechanical parameters that could enhance selection accuracy. Recent studies indicate that the stiffness (elasticity) of the zona pellucida (ZP) - the glycoprotein-rich extracellular matrix surrounding mammalian oocytes and embryos - correlates with embryo quality and developmental potential. However, current biomechanical characterization techniques - including micropipette aspiration, atomic force microscopy (AFM), microtactile sensors, and MEMS-based systems - either pose risks of mechanical damage or involve complex, time-consuming procedures unsuitable for clinical settings. Here, we introduce a novel approach leveraging fluidic force microscopy cantilevers to non-invasively evaluate embryo biomechanics. Our proof-of-concept study demonstrates rapid, precise stiffness profiling of intact mouse embryos (specifically ZP elasticity) in under one minute per embryo. Using gentle microsuction attachment with no chemical adhesives or rigid immobilization, the method preserves embryo integrity while providing reproducible elasticity measurements. This method combines the precision of AFM with minimal invasiveness, offering a promising new quantitative biomechanical indicator to augment clinical embryo assessment and paving the way for broader applications in reproductive biology.

biophysics↗

The molecular mechanism of load adaptation by branched actin networks

Branched actin networks are self-assembling molecular motors that move biological membranes and drive many important cellular processes. Load forces slow the growth and increase the density of these networks, but the molecular mechanisms governing this force response are not well understood. Here we use single-molecule imaging and AFM cantilever deflection to measure how applied forces affect each step in branched actin network assembly. Unexpectedly, force slows the rate of filament nucleation by promoting the interaction of nucleation promoting factors with actin filament ends, limiting branch formation. This inhibition is countered by an even larger force-induced drop in the rate of filament capping, resulting in a shift in the balance between nucleation and capping that increases network density. Remarkably, the force dependence of capping is identical to that of filament elongation because they require the same size gap to appear between the filament and load for insertion. These results provide direct evidence that Brownian Ratchets generate force and govern the load adaptation of branched actin networks.

biophysics↗