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    Mechanical properties of protein isopeptide tags for single-molecule force spectroscopy

    Zhiqi Hou1,2, Ping Yu1,2, Xingyu Qi1,2, Zhenyong Xue3, Hao Sun2, Zilong Guo2, Shimin Le1,*, and Hu Chen1,2,†

    • 1Research Institute for Biomimetics and Soft Matter, Fujian Provincial Key Lab for Soft Functional Materials Research, Department of Physics, Xiamen University, Xiamen 361005, China
    • 2Center of Biomedical Physics, Zhejiang Key Laboratory of Soft Matter Biomedical Materials, Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou 325000, China
    • 3School of Electronic and Electrical Engineering, Shangqiu Normal University, Shangqiu 476000, China

    • *Contact author: leshimin@xmu.edu.cn
    • †Contact author: chenhu@xmu.edu.cn

    Phys. Rev. Applied 26, 054008 – Published 3 November, 2026

    DOI: https://doi.org/10.1103/8bsh-l4g1

    This article was published on 3 November, 2026. Please update your links.

    Abstract

    Single-molecule force spectroscopy has revolutionized our understanding of protein mechanical mechanics by relying on versatile protein tags that enable specific tethering while providing unambiguous mechanical signatures. Here we characterize isopeptide bond-forming protein tags—the updated version of SpyTag-SpyCatcher (Spy003) and DogTag-DogCatcher (Dog)—as ideal multifunctional platforms that satisfy this need. Using magnetic tweezers, we demonstrate that these tags exhibit remarkably robust fingerprint signals when both N termini of the tag and catcher are stretched with characteristic critical forces (Spy003: 31.4 pN; Dog: 33.8 pN) and step sizes of approximately 4  nm across diverse experimental conditions including different buffers, salt concentrations (10–1000 mM NaCl), temperatures (23–36 °C), and pH values (pH 6–8). In particular, Dog exhibits local unfolding and refolding transitions of DogTag that are 6 times faster than those of Spy003, making it suitable for applications requiring high loading rates, while its compact hairpin structure minimizes structural perturbation when inserted into target proteins. We further proposed a variance-based force-calibration method that exploits the tags’ mechanical transitions to enable rapid, real-time force calibration during experiments, eliminating separate calibration routines. The combination of covalent tethering, environmental resilience, built-in calibration, and distinct mechanical signatures makes these tags powerful tools for studying protein mechanical mechanics in complex physiologically relevant environments.

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