Sethi Soumya, Xu Tao, Sarkar Aritra, Drees Christoph, Jacob Claire, Walther Andreas
Life-like Materials and Systems, Department of Chemistry, University of Mainz, Duesbergweg 10-14, 55128, Mainz, Germany.
Department of Biology, University of Mainz, Hanns-Dieter-Hüsch-Weg 15, 55128, Mainz, Germany.
Angew Chem Int Ed Engl. 2024 Dec 9;63(50):e202413983. doi: 10.1002/anie.202413983. Epub 2024 Oct 25.
DNA-based tension probes with precisely programmable force responses provide important insights into cellular mechanosensing. However, their degradability in cell culture limits their use for long-term imaging, for instance, when cells migrate, divide, and differentiate. This is a critical limitation for providing insights into mechanobiology for these longer-term processes. Here, we present DNA-based tension probes that are entirely designed based on the stereoisomer of biological D-DNA, i.e., L-DNA. We demonstrate that L-DNA tension probes are essentially indestructible by nucleases and provide days-long imaging without significant loss in image quality. We also show their superiority already for short imaging times commonly used for classical D-DNA tension probes. We showcase the potential of these resilient probes to image minute movements, and for generating long term force maps of single cells and of collectively migrating cell populations.
具有精确可编程力响应的基于DNA的张力探针为细胞机械传感提供了重要见解。然而,它们在细胞培养中的可降解性限制了其在长期成像中的应用,例如,当细胞迁移、分裂和分化时。对于深入了解这些长期过程的力学生物学而言,这是一个关键限制。在此,我们展示了完全基于生物D-DNA的立体异构体(即L-DNA)设计的基于DNA的张力探针。我们证明L-DNA张力探针基本上不会被核酸酶破坏,并能提供长达数天的成像,且图像质量不会有显著损失。我们还展示了它们在通常用于经典D-DNA张力探针的短成像时间内的优越性。我们展示了这些弹性探针在成像微小运动以及生成单细胞和集体迁移细胞群体的长期力图谱方面的潜力。