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Yanase, T.

Publications and source records attributed to Yanase, T..

2 recordsLinked to original sources

Computational design of membrane fusion proteins

The fusion of two distinct biological membranes is an evolutionarily conserved process essential to cellular organization and physiology. Membrane fusion is driven by the refolding of fusogenic proteins into low-energy postfusion states that overcome the energetic barrier to bilayer merger. Here we report a computational method for the design of synthetic fusogens inspired by the architecture of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) complex. Using machine learning-guided protein design to extensively remodel backbone geometry and sequence, we generated heterodimeric SNARE-like assemblies that efficiently catalyze cell-cell membrane fusion. These minimal two-component fusogens exhibit substantially higher fusion activity than native multisubunit SNARE complexes. Structural and functional analyses identify the key determinants required for fusogenic activity and reveal a modularity that enables control of fusion through chemically induced heterodimerization. In addition to cell-cell fusion, the synthetic fusogens drive fusion between endoplasmic reticulum and mitochondrial membranes from human cells, demonstrating their potential as tools for programmable manipulation of intracellular membranes. Together, these results establish a general framework for the rational design of synthetic fusogens and expand the toolkit for engineering membrane dynamics in living systems.

biochemistry↗

Programmable protein editing by split intein-mediated recombination

Biological regulation has long relied on modifying genes, transcripts, or protein abundance, yet direct rewriting of protein sequence after translation remains largely inaccessible. Here, we introduce a programmable protein editing platform based on split intein-mediated recombination, enabling precise excision and replacement of defined segments within mature proteins in living cells. By covalently exchanging a target segment with a donor-encoded sequence supplied in trans, this approach functions as a protein-level analogue of recombination, operating independently of transcription or translation. Using ultrafast and orthogonal split inteins, we demonstrate efficient protein recombination in mammalian cells, enabling single-amino acid substitutions, domain replacement, functional switching, and reprogramming of subcellular localization. This work establishes post-translational protein recombination as a general strategy for sequence-level control of protein function, expanding the conceptual and practical scope of biological editing beyond nucleic acids.

biochemistry↗