Application of single-molecule analysis to singularity phenomenon of cells.

large-scale analysis single-cell analysis single-molecule imaging singularity biology tau aggregation

Journal

Biophysics and physicobiology
ISSN: 2189-4779
Titre abrégé: Biophys Physicobiol
Pays: Japan
ID NLM: 101675089

Informations de publication

Date de publication:
2024
Historique:
received: 29 02 2024
accepted: 02 05 2024
medline: 23 8 2024
pubmed: 23 8 2024
entrez: 23 8 2024
Statut: epublish

Résumé

Single-molecule imaging in living cells is an effective tool for elucidating the mechanisms of cellular phenomena at the molecular level. However, the analysis was not designed for throughput and requires high expertise, preventing it from reaching large scale, which is necessary when searching for rare cells that induce singularity phenomena. To overcome this limitation, we have automated the imaging procedures by combining our own focusing device, artificial intelligence, and robotics. The apparatus, called automated in-cell single-molecule imaging system (AiSIS), achieves a throughput that is a hundred-fold higher than conventional manual imaging operations, enabling the analysis of molecular events by individual cells across a large population. Here, using AiSIS, we demonstrate the single-molecule imaging of molecular behaviors and reactions related to tau protein aggregation, which is considered a singularity phenomenon in neurological disorders. Changes in the dynamics and kinetics of molecular events were observed inside and on the basal membrane of cells after the induction of aggregation. Additionally, to detect rare cells based on the molecular behavior, we developed a method to identify the state of individual cells defined by the quantitative distribution of molecular mobility and clustering. Using this method, cellular variations in receptor behavior were shown to decrease following ligand stimulation. This cell state analysis based on large-scale single-molecule imaging by AiSIS will advance the study of molecular mechanisms causing singularity phenomena.

Identifiants

pubmed: 39175861
doi: 10.2142/biophysico.bppb-v21.s018
pii: JST.JSTAGE/biophysico/e211018
pmc: PMC11338674
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e211018

Informations de copyright

2024 THE BIOPHYSICAL SOCIETY OF JAPAN.

Déclaration de conflit d'intérêts

The authors declare no competing interests.

Auteurs

Michio Hiroshima (M)

Laboratory of Single Molecule Biology, Graduate School of Frontier Biosciences, Osaka University, Osaka 565-0871, Japan.
Laboratory for Cell Signaling Dynamics, RIKEN BDR, Osaka 565-0874, Japan.

Hiroko Bannai (H)

School of Advanced Science and Engineering, Department of Electrical Engineering and Biosciences, Waseda University, Shinjuku-ku, Tokyo 162-0056, Japan.

Gen Matsumoto (G)

Department of Neurological Disease Control, Osaka Metropolitan University Graduate School of Medicine, Osaka 545-8585, Japan.
Department of Anatomy and Neurobiology, Nagasaki University School of Medicine, Nagasaki 852-8523, Japan.

Masahiro Ueda (M)

Laboratory of Single Molecule Biology, Graduate School of Frontier Biosciences, Osaka University, Osaka 565-0871, Japan.
Laboratory for Cell Signaling Dynamics, RIKEN BDR, Osaka 565-0874, Japan.

Classifications MeSH