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Photoswitchable intein for light control of covalent protein binding and cleavage

Author

Listed:
  • Mikhail Baloban

    (Albert Einstein College of Medicine)

  • Kyrylo Yu. Manoilov

    (Albert Einstein College of Medicine)

  • Maksim M. Karasev

    (University of Helsinki)

  • Vladislav V. Verkhusha

    (Albert Einstein College of Medicine
    University of Helsinki)

  • Daria M. Shcherbakova

    (Albert Einstein College of Medicine)

Abstract

Precise control of covalent protein binding and cleavage in mammalian cells is crucial for manipulating cellular processes but remains challenging due to dark background, poor stability, low efficiency, or requirement of unnatural amino acids in current optogenetic tools. We introduce a photoswitchable intein (PS Intein) engineered by allosterically modulating a small autocatalytic gp41-1 intein with tandem Vivid photoreceptor. PS Intein exhibits superior functionality and low background in cells compared to existing tools. PS Intein-based systems enable light-induced covalent binding, cleavage, and release of proteins for regulating gene expression and cell fate. The high responsiveness and ability to integrate multiple inputs allow for intersectional cell targeting using cancer- and tumor microenvironment-specific promoters. PS Intein tolerates various fusions and insertions, facilitating its application in diverse cellular contexts. This versatile technology offers efficient light-controlled protein manipulation, providing a powerful tool for adding functionalities to proteins and precisely controlling protein networks in living cells.

Suggested Citation

  • Mikhail Baloban & Kyrylo Yu. Manoilov & Maksim M. Karasev & Vladislav V. Verkhusha & Daria M. Shcherbakova, 2025. "Photoswitchable intein for light control of covalent protein binding and cleavage," Nature Communications, Nature, vol. 16(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63595-9
    DOI: 10.1038/s41467-025-63595-9
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    References listed on IDEAS

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    1. Christopher H. Bowen & Cameron J. Sargent & Ao Wang & Yaguang Zhu & Xinyuan Chang & Jingyao Li & Xinyue Mu & Jonathan M. Galazka & Young-Shin Jun & Sinan Keten & Fuzhong Zhang, 2021. "Microbial production of megadalton titin yields fibers with advantageous mechanical properties," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
    2. Liyuan Zhu & Harold M. McNamara & Jared E. Toettcher, 2023. "Light-switchable transcription factors obtained by direct screening in mammalian cells," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    3. Zhong Yao & Farzaneh Aboualizadeh & Jason Kroll & Indira Akula & Jamie Snider & Anna Lyakisheva & Priscilla Tang & Max Kotlyar & Igor Jurisica & Mike Boxem & Igor Stagljar, 2020. "Split Intein-Mediated Protein Ligation for detecting protein-protein interactions and their inhibition," Nature Communications, Nature, vol. 11(1), pages 1-14, December.
    4. Filipe Pinto & Ella Lucille Thornton & Baojun Wang, 2020. "An expanded library of orthogonal split inteins enables modular multi-peptide assemblies," Nature Communications, Nature, vol. 11(1), pages 1-15, December.
    5. Agnieszka A. Gil & César Carrasco-López & Liyuan Zhu & Evan M. Zhao & Pavithran T. Ravindran & Maxwell Z. Wilson & Alexander G. Goglia & José L. Avalos & Jared E. Toettcher, 2020. "Optogenetic control of protein binding using light-switchable nanobodies," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
    6. Hannes M. Beyer & Sant Kumar & Marius Nieke & Carroll M. C. Diehl & Kun Tang & Sara Shumka & Cha San Koh & Christian Fleck & Jamie A. Davies & Mustafa Khammash & Matias D. Zurbriggen, 2024. "Genetically-stable engineered optogenetic gene switches modulate spatial cell morphogenesis in two- and three-dimensional tissue cultures," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    7. Navaneethan Palanisamy & Anna Degen & Anna Morath & Jara Ballestin Ballestin & Claudia Juraske & Mehmet Ali Öztürk & Georg A. Sprenger & Jung-Won Youn & Wolfgang W. Schamel & Barbara Di Ventura, 2019. "Split intein-mediated selection of cells containing two plasmids using a single antibiotic," Nature Communications, Nature, vol. 10(1), pages 1-15, December.
    8. Kumi Morikawa & Kazuhiro Furuhashi & Carmen Sena-Tomas & Alvaro L. Garcia-Garcia & Ramsey Bekdash & Alison D. Klein & Nicholas Gallerani & Hannah E. Yamamoto & Seon-Hye E. Park & Grant S. Collins & Fu, 2020. "Photoactivatable Cre recombinase 3.0 for in vivo mouse applications," Nature Communications, Nature, vol. 11(1), pages 1-11, December.
    9. Nathaniel Jillette & Menghan Du & Jacqueline Jufen Zhu & Peter Cardoz & Albert Wu Cheng, 2019. "Split selectable markers," Nature Communications, Nature, vol. 10(1), pages 1-8, December.
    10. Hao-Shan Chen & Xiao-Long Zhang & Rong-Rong Yang & Guang-Ling Wang & Xin-Yue Zhu & Yuan-Fang Xu & Dan-Yang Wang & Na Zhang & Shou Qiu & Li-Jie Zhan & Zhi-Ming Shen & Xiao-Hong Xu & Gang Long & Chun Xu, 2022. "An intein-split transactivator for intersectional neural imaging and optogenetic manipulation," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
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