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Sigma Proteins: Evolution of the Concept of Sigma Receptors

  • Felix J. Kim
  • Gavril W. Pasternak

Part of the Handbook of Experimental Pharmacology book series (HEP, volume 244)

Table of contents

  1. Front Matter
    Pages i-viii
  2. Andrew Kruse
    Pages 13-25
  3. Erik Laurini, Domenico Marson, Maurizio Fermeglia, Sabrina Pricl
    Pages 27-50
  4. Tangui Maurice, Nino Goguadze
    Pages 81-108
  5. Saïd Kourrich
    Pages 109-130
  6. Manuel Merlos, Luz Romero, Daniel Zamanillo, Carlos Plata-Salamán, José Miguel Vela
    Pages 131-161
  7. Jonathan L. Katz, Takato Hiranita, Weimin C. Hong, Martin O. Job, Christopher R. McCurdy
    Pages 177-218
  8. Valentina Sabino, Pietro Cottone
    Pages 219-236
  9. Felix J. Kim, Christina M. Maher
    Pages 237-308
  10. Chenbo Zeng, Elizabeth S. McDonald, Robert H. Mach
    Pages 309-330

About this book

Introduction

Two sigma receptor subtypes have been proposed, sigma1 and 2. Much of our understanding of this system is based on biochemical and pharmacological characterization of the cloned sigma1 receptor subtype (Sigma1). It has become clear that sigma receptors are not canonical receptors. Sigma1 is highly conserved among mammalian species, however, it does not share significant homology with any other mammalian protein. Although a range of structurally diverse small molecules bind Sigma1 with high affinity, and it has been associated with a broad range of signaling systems, Sigma1 itself has no known signaling or enzymatic activity. The evolution of this field over nearly four decades has more recently led to a fundamental shift in the concept of “sigma receptors” to what may more accurately and generally be called sigma proteins. Largely based on traditional pharmacologic approaches, the Sigma1 protein has been associated with a broad range of signaling systems, including G-protein coupled receptors, NMDA receptors, and ion channels. Sigma proteins have been linked to a range of physiological processes, including intracellular calcium signaling, neuroprotection, learning, memory, and cognition. Emerging genetic, clinical, and mechanism focused molecular pharmacology data demonstrate the involvement of proteins in a range of pathophysiologies and disorders including neurodegenerative disease, pain, addiction, psychomotor stimulant abuse, and cancer. However, an understanding of the physiological role of sigma proteins has remained elusive. Emerging data associate Sigma1 with chaperone-like activities or molecular scaffold functions. This book aims to provide an updated perspective on this rapidly evolving field undergoing changes in fundamental concepts of key importance to the discipline of pharmacology. It focusses on the reported roles of sigma proteins in pathophysiology and on emergent therapeutic initiatives.

Keywords

Chaperone Neurodegenerative disease Pain Pathophysiology Protein homeostasis Scaffold

Editors and affiliations

  • Felix J. Kim
    • 1
  • Gavril W. Pasternak
    • 2
  1. 1.Pharmacology & PhysiologyDrexel University College of MedicinePhiladelphiaUSA
  2. 2.Molecular Pharmacology and ChemistryMemorial Sloan-Kettering Cancer CenterNew YorkUSA

Bibliographic information

  • DOI https://doi.org/10.1007/978-3-319-65853-7
  • Copyright Information Springer International Publishing AG 2017
  • Publisher Name Springer, Cham
  • eBook Packages Biomedical and Life Sciences
  • Print ISBN 978-3-319-65851-3
  • Online ISBN 978-3-319-65853-7
  • Series Print ISSN 0171-2004
  • Series Online ISSN 1865-0325
  • Buy this book on publisher's site
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