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Turn-on protein switches for controlling actin binding in cells.
Effiong, Unyime M; Khairandish, Hannah; Ramirez-Velez, Isabela; Wang, Yanran; Belardi, Brian.
Afiliação
  • Effiong UM; McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Khairandish H; McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Ramirez-Velez I; McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Wang Y; McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA.
  • Belardi B; McKetta Department of Chemical Engineering, The University of Texas at Austin, Austin, TX, 78712, USA. bdb@che.utexas.edu.
Nat Commun ; 15(1): 5840, 2024 Jul 11.
Article em En | MEDLINE | ID: mdl-38992021
ABSTRACT
Within a shared cytoplasm, filamentous actin (F-actin) plays numerous and critical roles across the cell body. Cells rely on actin-binding proteins (ABPs) to organize F-actin and to integrate its polymeric characteristics into diverse cellular processes. Yet, the multitude of ABPs that engage with and shape F-actin make studying a single ABP's influence on cellular activities a significant challenge. Moreover, without a means of manipulating actin-binding subcellularly, harnessing the F-actin cytoskeleton for synthetic biology purposes remains elusive. Here, we describe a suite of designed proteins, Controllable Actin-binding Switch Tools (CASTs), whose actin-binding behavior can be controlled with external stimuli. CASTs were developed that respond to different external inputs, providing options for turn-on kinetics and enabling orthogonality and multiplexing. Being genetically encoded, we show that CASTs can be inserted into native protein sequences to control F-actin association locally and engineered into structures to control cell and tissue shape and behavior.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ligação Proteica / Citoesqueleto de Actina / Actinas / Proteínas dos Microfilamentos Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ligação Proteica / Citoesqueleto de Actina / Actinas / Proteínas dos Microfilamentos Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article