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Lipids in Protein Misfolding

  • Olga Gursky

Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 855)

Table of contents

  1. Front Matter
    Pages i-xiii
  2. Vladimir N. Uversky
    Pages 33-66
  3. Isabel Morgado, Megan Garvey
    Pages 67-94
  4. Sanghamitra Singh, Saurabh Trikha, Diti Chatterjee Bhowmick, Anjali A. Sarkar, Aleksandar M. Jeremic
    Pages 95-116
  5. Wilfredo Colón, J. Javier Aguilera, Saipraveen Srinivasan
    Pages 117-134
  6. Galyna Gorbenko, Valeriya Trusova, Mykhailo Girych, Emi Adachi, Chiharu Mizuguchi, Hiroyuki Saito
    Pages 135-155
  7. Timothy M. Ryan, Yee-Foong Mok, Geoffrey J. Howlett, Michael D. W. Griffin
    Pages 157-174
  8. Elena I. Leonova, Oxana V. Galzitskaya
    Pages 241-258
  9. Back Matter
    Pages 259-260

About this book

Introduction

This book addresses molecular mechanisms of protein misfolding and the role of lipids and related molecules in these complex processes. The focus is on the biophysical and structural studies of proteins that are involved in major human disorders such as Alzheimer’s disease, systemic amyloidoses, diabetes II, inflammation and atherosclerosis. Misfolding often results from protein mutations or modifications. Misfolding of membrane proteins can cause topological changes that target the proteins for degradation. Misfolding of soluble globular proteins and peptides converts them into β-sheet-rich aggregates and amyloid fibrils. This process can disrupt the structural integrity of the lipid membranes and thereby contribute to amyloid toxicity. In turn, lipids and lipid-associated molecules such as apolipoproteins and heparan sulfate proteoglycans, which are ubiquitous constituents of amyloid plaques, can influence protein misfolding via diverse mechanisms that are addressed in this book.

The book features chapters describing the role of lipids in the misfolding of a wide range of proteins, including small peptides, globular proteins, lipid surface-binding proteins, and integral membrane proteins. The role of individual lipid molecules, lipid surfaces, and the membrane field is addressed, including specific and non-specific interactions with protein oligomers and mature fibrils. Distinct effects of various lipids on the nucleation and growth of amyloid fibrils are discussed. Modern computational approaches to the analysis of amyloid formation are addressed.  The book should be useful to experts in the field but is also accessible to novices.

Keywords

amyloid formation biophysical and structural approaches molecular mechanisms of protein misfolding protein misfolding in amyloid diseases protein-lipid interactions

Editors and affiliations

  • Olga Gursky
    • 1
  1. 1.Dept. of Physiology and BiophysicsBoston University School of MedicineBostonUSA

Bibliographic information

  • DOI https://doi.org/10.1007/978-3-319-17344-3
  • Copyright Information Springer International Publishing Switzerland 2015
  • Publisher Name Springer, Cham
  • eBook Packages Biomedical and Life Sciences
  • Print ISBN 978-3-319-17343-6
  • Online ISBN 978-3-319-17344-3
  • Series Print ISSN 0065-2598
  • Series Online ISSN 2214-8019
  • Buy this book on publisher's site
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