Literature DB >> 21840295

Physical-chemical principles underlying RTK activation, and their implications for human disease.

Lijuan He1, Kalina Hristova.   

Abstract

RTKs, the second largest family of membrane receptors, exert control over cell proliferation, differentiation and migration. In recent years, our understanding of RTK structure and activation in health and disease has skyrocketed. Here we describe experimental approaches used to interrogate RTKs, and we review the quantitative biophysical frameworks and structural considerations that shape our understanding of RTK function. We discuss current knowledge about RTK interactions, focusing on the role of different domains in RTK homodimerization, and on the importance and challenges in RTK heterodimerization studies. We also review our understanding of pathogenic RTK mutations, and the underlying physical-chemical causes for the pathologies. This article is part of a Special Issue entitled: Protein Folding in Membranes. Copyright Â
© 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21840295      PMCID: PMC3276721          DOI: 10.1016/j.bbamem.2011.07.044

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  162 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

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Journal:  Proc Natl Acad Sci U S A       Date:  1979-07       Impact factor: 11.205

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Journal:  Hum Mol Genet       Date:  2004-07-28       Impact factor: 6.150

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Journal:  J Cell Sci       Date:  1979-02       Impact factor: 5.285

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Journal:  J Cell Sci       Date:  1979-02       Impact factor: 5.285

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  27 in total

1.  The FRET signatures of noninteracting proteins in membranes: simulations and experiments.

Authors:  Christopher King; Sarvenaz Sarabipour; Patrick Byrne; Daniel J Leahy; Kalina Hristova
Journal:  Biophys J       Date:  2014-03-18       Impact factor: 4.033

2.  Structure of FGFR3 transmembrane domain dimer: implications for signaling and human pathologies.

Authors:  Eduard V Bocharov; Dmitry M Lesovoy; Sergey A Goncharuk; Marina V Goncharuk; Kalina Hristova; Alexander S Arseniev
Journal:  Structure       Date:  2013-10-10       Impact factor: 5.006

3.  Quantifying the Interaction between EGFR Dimers and Grb2 in Live Cells.

Authors:  Nuala Del Piccolo; Kalina Hristova
Journal:  Biophys J       Date:  2017-07-19       Impact factor: 4.033

4.  A New Method to Study Heterodimerization of Membrane Proteins and Its Application to Fibroblast Growth Factor Receptors.

Authors:  Nuala Del Piccolo; Sarvenaz Sarabipour; Kalina Hristova
Journal:  J Biol Chem       Date:  2016-12-07       Impact factor: 5.157

5.  The SAM domain inhibits EphA2 interactions in the plasma membrane.

Authors:  Deo R Singh; Fozia Ahmed; Michael D Paul; Manasee Gedam; Elena B Pasquale; Kalina Hristova
Journal:  Biochim Biophys Acta Mol Cell Res       Date:  2016-10-21       Impact factor: 4.739

6.  MET-activating Residues in the B-repeat of the Listeria monocytogenes Invasion Protein InlB.

Authors:  Willem M Bleymüller; Nina Lämmermann; Maria Ebbes; Daniel Maynard; Christina Geerds; Hartmut H Niemann
Journal:  J Biol Chem       Date:  2016-10-27       Impact factor: 5.157

7.  Understanding the FRET Signatures of Interacting Membrane Proteins.

Authors:  Christopher King; Valerica Raicu; Kalina Hristova
Journal:  J Biol Chem       Date:  2017-02-09       Impact factor: 5.157

8.  Strong dimerization of wild-type ErbB2/Neu transmembrane domain and the oncogenic Val664Glu mutant in mammalian plasma membranes.

Authors:  Jesse Placone; Lijuan He; Nuala Del Piccolo; Kalina Hristova
Journal:  Biochim Biophys Acta       Date:  2014-03-11

9.  Revisiting a controversy: The effect of EGF on EGFR dimer stability.

Authors:  Deo R Singh; Christopher King; Matt Salotto; Kalina Hristova
Journal:  Biochim Biophys Acta Biomembr       Date:  2019-07-08       Impact factor: 3.747

10.  The RTK Interactome: Overview and Perspective on RTK Heterointeractions.

Authors:  Michael D Paul; Kalina Hristova
Journal:  Chem Rev       Date:  2018-12-27       Impact factor: 60.622

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