Membrane and Actin Tethering Transitions Help IQGAP1 Coordinate GTPase and Lipid Messenger Signaling.

Autor:	Trenton NJ; Department of Bioengineering, Rice University, Houston, Texas., McLaughlin RT; Department of Bioengineering, Rice University, Houston, Texas; Graduate Program in Systems, Synthetic and Physical Biology, Rice University, Houston, Texas., Bellamkonda SK; Department of Bioengineering, Rice University, Houston, Texas., Tsao DS; Department of Bioengineering, Rice University, Houston, Texas., Rodzinski A; Department of Bioengineering, Rice University, Houston, Texas., Mace EM; Department of Pediatrics, Columbia University Irving Medical Center, New York, New York., Orange JS; Department of Pediatrics, Columbia University Irving Medical Center, New York, New York., Schweikhard V; Department of Bioengineering, Rice University, Houston, Texas., Diehl MR; Department of Bioengineering, Rice University, Houston, Texas; Graduate Program in Systems, Synthetic and Physical Biology, Rice University, Houston, Texas; Department of Chemistry, Rice University, Houston, Texas. Electronic address: diehl@rice.edu.
Jazyk:	angličtina
Zdroj:	Biophysical journal [Biophys J] 2020 Feb 04; Vol. 118 (3), pp. 586-599. Date of Electronic Publication: 2019 Dec 31.
DOI:	10.1016/j.bpj.2019.12.023
Abstrakt:	The coordination of lipid messenger signaling with cytoskeletal regulation is central to many organelle-specific regulatory processes. This coupling often depends on the function of multidomain scaffolds that orchestrate transient interactions among multiple signaling intermediates and regulatory proteins on organelles. The number of possible scaffold interaction partners and the ability for these interactions to occur at different timescales makes investigations of scaffold functions challenging. This work employs live cell imaging to probe how the multidomain scaffold IQ motif containing GTPase activating protein 1 (IQGAP1) coordinates the activities of proteins affecting local actin polymerization, membrane processing, and phosphoinositide signaling. Using endosomes that are confined by a local actin network as a model system, we demonstrate that IQGAP1 can transition between different actin and endosomal membrane tethered states. Fast scaffold binding/disassociation transitions are shown to be driven by interactions between C-terminal scaffold domains and Rho GTPases at the membrane. Fluctuations in these binding modes are linked to negative regulation of actin polymerization. Although this control governs core elements of IQGAP1 dynamics, actin binding by the N-terminal calponin homology domain of the scaffold is shown to help the scaffold track the temporal development of endosome membrane markers, implying actin associations bolster membrane and actin coordination. Importantly, these effects are not easily distilled purely through standard (static) co-localization analyses or traditional pathway perturbations methods and were resolved by performing dynamic correlation and multiple regression analyses of IQGAP1 scaffold mutants. Using these capabilities with pharmacological inhibition, we provide evidence that membrane tethering is dependent on the activities of the lipid kinase phosphoinositide 3-kinase in addition to the Rho GTPases Rac1 and Cdc42. Overall, these methods and results point to a scaffold tethering mechanism that allows IQGAP1 to help control the amplitude of phosphoinositide lipid messenger signaling by coordinating signaling intermediate activities with the development and disassembly of local actin cytoskeletal networks. (Copyright © 2020 Biophysical Society. Published by Elsevier Inc. All rights reserved.)
Databáze:	MEDLINE
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