Accurate drift-invariant single-molecule force calibration using the Hadamard variance.

IF 3.2 3区 生物学 Q2 BIOPHYSICS Biophysical journal Pub Date : 2024-11-19 Epub Date: 2024-10-29 DOI:10.1016/j.bpj.2024.10.008
Stefanie D Pritzl, Alptuğ Ulugöl, Caroline Körösy, Laura Filion, Jan Lipfert
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Abstract

Single-molecule force spectroscopy (SMFS) techniques play a pivotal role in unraveling the mechanics and conformational transitions of biological macromolecules under external forces. Among these techniques, multiplexed magnetic tweezers (MT) are particularly well suited to probe very small forces, ≤1 pN, critical for studying noncovalent interactions and regulatory conformational changes at the single-molecule level. However, to apply and measure such small forces, a reliable and accurate force-calibration procedure is crucial. Here, we introduce a new approach to calibrate MT based on thermal motion using the Hadamard variance (HV). To test our method, we perform bead-tether Brownian dynamics simulations that mimic our experimental system and compare the performance of the HV method against two established techniques: power spectral density (PSD) and Allan variance (AV) analyses. Our analysis includes an assessment of each method's ability to mitigate common sources of additive noise, such as white and pink noise, as well as drift, which often complicate experimental data analysis. We find that the HV method exhibits overall similar or higher precision and accuracy, yielding lower force estimation errors across a wide range of signal-to-noise ratios (SNRs) and drift speeds compared with the PSD and AV methods. Notably, the HV method remains robust against drift, maintaining consistent uncertainty levels across the entire studied SNR and drift speed spectrum. We also explore the HV method using experimental MT data, where we find overall smaller force estimation errors compared with PSD and AV approaches. Overall, the HV method offers a robust method for achieving sub-pN resolution and precision in multiplexed MT measurements. Its potential extends to other SMFS techniques, presenting exciting opportunities for advancing our understanding of mechanosensitivity and force generation in biological systems. To make our methods widely accessible to the research community, we provide a well-documented Python implementation of the HV method as an extension to the Tweezepy package.

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利用哈达玛方差进行精确的漂移不变单分子力校准
单分子力谱(SMFS)技术在揭示生物大分子在外力作用下的力学和构象转变方面发挥着举足轻重的作用。在这些技术中,多路复用磁镊(MT)尤其适合探测≤1 pN的极小力,这对研究单分子水平的非共价相互作用和调控构象变化至关重要。然而,要应用和测量如此小的力,可靠而准确的力校准程序至关重要。在此,我们介绍一种基于热运动的哈达玛方差(HV)校准 MT 的新方法。为了测试我们的方法,我们进行了模拟实验系统的珠系布朗动力学模拟,并将 HV 方法的性能与两种成熟技术进行了比较:功率谱密度 (PSD) 和阿伦方差 (AV) 分析。我们的分析包括评估每种方法缓解白噪声和粉红噪声等常见加性噪声源以及漂移的能力,漂移通常会使实验数据分析复杂化。我们发现,与 PSD 和 AV 方法相比,HV 方法在总体上表现出相似或更高的精度和准确性,在广泛的信噪比 (SNR) 和漂移速度范围内产生更低的力估算误差。值得注意的是,HV 方法对漂移保持稳健,在整个研究的信噪比和漂移速度范围内保持一致的不确定性水平。我们还利用 MT 实验数据探索了 HV 方法,发现与 PSD 和 AV 方法相比,HV 方法的力估算误差总体较小。总之,HV 方法为在多路 MT 测量中实现亚 pN 分辨率和精度提供了一种稳健的方法。它的潜力还可扩展到其他 SMFS 技术,为我们进一步了解生物系统的机械敏感性和力的产生提供了令人兴奋的机会。为了使我们的方法能被研究界广泛使用,我们提供了 HV 方法的 Python 实现,作为 Tweezepy 软件包的扩展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biophysical journal
Biophysical journal 生物-生物物理
CiteScore
6.10
自引率
5.90%
发文量
3090
审稿时长
2 months
期刊介绍: BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.
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