mTORC1は,チューニング・クラウンディングにより,相分離と細胞質の生物物理的特性を制御する
M Delarue1, G P Brittingham1, S Pfeffer2
1Institute for Systems Genetics, New York University Langone Health, New York, NY 10016, USA.
Cell
|June 26, 2018
まとめ
遺伝子でコードされたマルチメリックナノ粒子は,mTORC1経路がリボソーム濃度を調節することによって細胞の混雑を制御する方法を明らかにしています. これは細胞内の物理的性質と相分離に影響します.
科学分野:
- 細胞生物物理学
- 分子生物学
- システム生物学
背景:
- マクロ分子混雑は細胞の反応率と物理的性質に大きく影響する.
- 細胞の混雑を制御する正確なメカニズムは ほとんど不明です
研究 の 目的:
- 細胞内のマクロ分子混雑の規制メカニズムを調査する.
- 細胞質の性質を調節する mTORC1 経路の役割を理解する.
主な方法:
- トラッキングのための遺伝子コード化されたマルチメリックナノ粒子 (GEM) の開発.
- GEMを遺伝子と薬理学的方法と組み合わせる
- 粒子と分子運動の有効拡散係数を測定する.
主要な成果:
- mTORC1経路は,リボソーム濃度の変化によって≥20 nmの微粒子の拡散を2倍以上調整する.
- 分子の運動に対する有意な影響は観察されなかった.
- リボソーム濃度の変化は,in vitroとin vivoの両方で相分離に影響を与えました.
結論:
- mTORC1経路は,細胞質のメソスケール生物物理的特性を制御する上で重要な役割を果たします.
- リボソーム濃度はmTORC1によって調節され,細胞質の特性や生物分子凝縮に影響する重要な要因である.
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