Institute of Physiology II, University of Münster, 48149, Münster, Germany.
Institute of Biophysics, University of Bremen, 28359, Bremen, Germany.
Sci Rep. 2017 Jul 11;7(1):5117. doi: 10.1038/s41598-017-05383-0.
We present a procedure that allows a reliable determination of the elastic (Young's) modulus of soft samples, including living cells, by atomic force microscopy (AFM). The standardized nanomechanical AFM procedure (SNAP) ensures the precise adjustment of the AFM optical lever system, a prerequisite for all kinds of force spectroscopy methods, to obtain reliable values independent of the instrument, laboratory and operator. Measurements of soft hydrogel samples with a well-defined elastic modulus using different AFMs revealed that the uncertainties in the determination of the deflection sensitivity and subsequently cantilever's spring constant were the main sources of error. SNAP eliminates those errors by calculating the correct deflection sensitivity based on spring constants determined with a vibrometer. The procedure was validated within a large network of European laboratories by measuring the elastic properties of gels and living cells, showing that its application reduces the variability in elastic moduli of hydrogels down to 1%, and increased the consistency of living cells elasticity measurements by a factor of two. The high reproducibility of elasticity measurements provided by SNAP could improve significantly the applicability of cell mechanics as a quantitative marker to discriminate between cell types and conditions.
我们提出了一种通过原子力显微镜(AFM)可靠地测定软样品(包括活细胞)弹性(杨氏)模量的方法。标准化纳米力学 AFM 程序(SNAP)确保了 AFM 光学杠杆系统的精确调整,这是所有类型力谱法的前提条件,可获得独立于仪器、实验室和操作人员的可靠值。使用不同的 AFM 对具有明确定义弹性模量的软水凝胶样品进行测量表明,在确定挠度灵敏度以及随后的悬臂梁弹簧常数时的不确定度是误差的主要来源。SNAP 通过根据振速计确定的弹簧常数计算正确的挠度灵敏度来消除这些误差。该程序通过测量凝胶和活细胞的弹性特性,在一个大型的欧洲实验室网络中得到了验证,结果表明,该程序的应用将水凝胶弹性模量的可变性降低到 1%,并将活细胞弹性测量的一致性提高了两倍。SNAP 提供的弹性测量的高重现性可以显著提高细胞力学作为定量标记物的适用性,以区分细胞类型和条件。