The scaffolding protein IQGAP1 enhances EGFR signaling by promoting oligomerization and preventing degradation

IQGAP1 is a large, multi-domain scaffold that connects and modulates different signaling networks including the one initiated by epidermal growth factor (EGF). In this study, we have used live cell fluorescence imaging methods along with other biochemical techniques to follow the mechanisms used by IQGAP1 to enhance EGF signaling. We show that IQGAP1 enhances EGF signaling by promoting the oligomerization of its receptor, EGFR, upon EGF addition along with concurrent IQGAP oligomerization. Using cellular markers, we find that IQGAP1 promotes the plasma membrane localization of EGFR and promotes association to one of its phosphoinositide lipid pathway ligands, PI(3,4,5)P<sub>3</sub>. Additionally, we find that binding of EGFR to IQGAP1 protects EGFR from lysosomal degradation. Taken together, our results show that IQGAP1 enhances EGF-mediated pathway progression through mechanisms that augment simple scaffolding activities.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2024-09-30
DOI
https://doi.org/10.1016/j.jbc.2024.107844
Citations
2
Primary Topic
Ubiquitin and proteasome pathways
Type
article
Field-Weighted Citation Impact
0.47

Funders

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article

The scaffolding protein IQGAP1 enhances EGFR signaling by promoting oligomerization and preventing degradation

Suzanne Scarlata, Arne Gericke, V. Siddartha Yerramilli, Jessica Reisinger et al.
2 citations
Journal of Biological Chemistry
Ubiquitin and proteasome pathways
0.47
article

The scaffolding protein IQGAP1 enhances EGFR signaling by promoting oligomerization and preventing degradation

Suzanne Scarlata, Arne Gericke, V. Siddartha Yerramilli, Jessica Reisinger, Guanyu Lin, Karin Plante, Samantha K. Lindberg, Alonzo H. Ross, Rachel M. Hemmerlin
article en
2 citations

Abstract

IQGAP1 is a large, multi-domain scaffold that connects and modulates different signaling networks including the one initiated by epidermal growth factor (EGF). In this study, we have used live cell fluorescence imaging methods along with other biochemical techniques to follow the mechanisms used by IQGAP1 to enhance EGF signaling. We show that IQGAP1 enhances EGF signaling by promoting the oligomerization of its receptor, EGFR, upon EGF addition along with concurrent IQGAP oligomerization. Using cellular markers, we find that IQGAP1 promotes the plasma membrane localization of EGFR and promotes association to one of its phosphoinositide lipid pathway ligands, PI(3,4,5)P<sub>3</sub>. Additionally, we find that binding of EGFR to IQGAP1 protects EGFR from lysosomal degradation. Taken together, our results show that IQGAP1 enhances EGF-mediated pathway progression through mechanisms that augment simple scaffolding activities.

Journal of Biological ChemistryVol. 300(11)
Worcester Polytechnic Institute (US), University of Massachusetts Chan Medical School (US)
National Science Foundation, Division of Chemistry
Zero hunger
Openalex Percentile: Top 35%
Ubiquitin and proteasome pathways
0.47
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