Dual compartment utility of BRET-based biosensors for PPP2R5A/B56α, a cancer-associated B regulatory subunit of PP2A

Protein phosphatase 2A (PP2A), a pivotal serine/threonine phosphatase, plays a crucial role in cellular regulation and tumor suppression. Dysregulation of PP2A complex, particularly the Aα subunit and B56 family, is linked to malignancies through altered substrate interactions, exemplified by c-MYC dynamics. Given the challenges in identifying PP2A substrates-owing to the enzyme's expansive substrate range, transient interaction profiles, and complex regulatory mechanisms-we employed bioluminescence resonance energy transfer (BRET) sensors. These advanced molecular tools facilitate the real-time detection of protein-protein interactions within live cells. This investigation details the creation and application of a novel PPP2R5A (B56α) BRET sensor tailored for cytosolic and nuclear environments, effectively distinguishing specific PP2A interactions. The nuclear sensor, enhanced with a nuclear localization signal, enabled probing of targets like c-MYC. The dual compartmental utility of these sensors underscores their significant potential in elucidating PP2A's regulatory roles and their implications in oncogenesis. Our study highlights the efficacy of BRET sensors in formulating precision therapeutic strategies. This advancement provides a robust framework for deeper investigations into the multifaceted roles of PP2A in both normal physiological and pathological contexts, paving the way for future explorations into its intricate molecular interactions.

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Publication Details

Journal
BioTechniques
Published
2025-04-03
DOI
https://doi.org/10.1080/07366205.2025.2523093
Primary Topic
Protein Kinase Regulation and GTPase Signaling
Type
article
Field-Weighted Citation Impact
0.00

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article

Dual compartment utility of BRET-based biosensors for PPP2R5A/B56α, a cancer-associated B regulatory subunit of PP2A

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BioTechniques
Protein Kinase Regulation and GTPase Signaling
article

Dual compartment utility of BRET-based biosensors for PPP2R5A/B56α, a cancer-associated B regulatory subunit of PP2A

Hirofumi Yamauchi, Mina Yoshida, Nobukata Shinohara, Atsuro Oishi, Marimu Sakumoto, Ryoichi Maenosono, Kazuki Nishimura, Asuka Kawachi, Miki Nagase, Michiko Kurikawa, Aiko Nakayama, Takahiro Nishino, Akihide Yoshimi, Motoaki HANZAWA, Shingo Yano, Rei Kudo, Junko Mukohyama, Tomoya Muto, Masahiko Ajiro, M Koizumi, Takuya Izumi-Tamura
article en

Abstract

Protein phosphatase 2A (PP2A), a pivotal serine/threonine phosphatase, plays a crucial role in cellular regulation and tumor suppression. Dysregulation of PP2A complex, particularly the Aα subunit and B56 family, is linked to malignancies through altered substrate interactions, exemplified by c-MYC dynamics. Given the challenges in identifying PP2A substrates-owing to the enzyme's expansive substrate range, transient interaction profiles, and complex regulatory mechanisms-we employed bioluminescence resonance energy transfer (BRET) sensors. These advanced molecular tools facilitate the real-time detection of protein-protein interactions within live cells. This investigation details the creation and application of a novel PPP2R5A (B56α) BRET sensor tailored for cytosolic and nuclear environments, effectively distinguishing specific PP2A interactions. The nuclear sensor, enhanced with a nuclear localization signal, enabled probing of targets like c-MYC. The dual compartmental utility of these sensors underscores their significant potential in elucidating PP2A's regulatory roles and their implications in oncogenesis. Our study highlights the efficacy of BRET sensors in formulating precision therapeutic strategies. This advancement provides a robust framework for deeper investigations into the multifaceted roles of PP2A in both normal physiological and pathological contexts, paving the way for future explorations into its intricate molecular interactions.

BioTechniquesVol. 77(4)
Jikei University School of Medicine (JP), Kyorin University (JP), The University of Tokyo (JP)
Takeda Science Foundation, Cell Science Research Foundation, Asahi Glass Foundation, Uehara Memorial Foundation, Takahashi Industrial and Economic Research Foundation, Japan Agency for Medical Research and Development, Vehicle Racing Commemorative Foundation, Kawano Masanori Memorial Public Interest Incorporated Foundation, Precise Measurement Technology Promotion Foundation, Japan Foundation for Pediatric Research, Hokuto Foundation for Bioscience, Mitsubishi Foundation, Foundation for Promotion of Cancer Research, Murata Science Foundation, Research Foundation for Opto-Science and Technology
Good health and well-being
Openalex Percentile: Top 86%
Protein Kinase Regulation and GTPase Signaling
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