Literature DB >> 15980600

Quasielastic light scattering for protein assembly studies.

Aleksey Lomakin1, David B Teplow, George B Benedek.   

Abstract

Quasielastic light scattering (QLS) spectroscopy is an optical method for the determination of diffusion coefficients of particles in solution. In this chapter, we discuss the principles and practice of QLS with respect to protein assembly reactions. Particles undergoing Brownian motion produce fluctuations in scattered light intensity. We describe how the temporal correlation function of these fluctuations can be measured and how this correlation function provides information about the distribution of diffusion coefficients of the particles in solution. We discuss the intricacies of deconvolution of the correlation function and the assumptions incorporated into data analysis procedures. We explain how the Stokes-Einstein relationship can be used to convert distributions of diffusion coefficients into distributions of particle size. Noninvasive observation of the temporal evolution of particles sizes provides a powerful tool for studying protein aggregation and self-assembly. We use examples from studies of Abeta fibrillogenesis to illustrate QLS application for understanding the molecular mechanisms of the nucleation and growth of amyloid fibrils.

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Year:  2005        PMID: 15980600     DOI: 10.1385/1-59259-874-9:153

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  10 in total

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2.  Impact of sequence on the molecular assembly of short amyloid peptides.

Authors:  Victoria A Wagoner; Mookyung Cheon; Iksoo Chang; Carol K Hall
Journal:  Proteins       Date:  2014-02-18

3.  A Microfluidic Platform for Real-Time Detection and Quantification of Protein-Ligand Interactions.

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5.  Biophysical characterization of Abeta42 C-terminal fragments: inhibitors of Abeta42 neurotoxicity.

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6.  C-terminal turn stability determines assembly differences between Aβ40 and Aβ42.

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Review 7.  Alpha crystallin: the quest for a homogeneous quaternary structure.

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8.  Gly25-Ser26 amyloid β-protein structural isomorphs produce distinct Aβ42 conformational dynamics and assembly characteristics.

Authors:  Robin Roychaudhuri; Aleksey Lomakin; Summer Bernstein; Xueyun Zheng; Margaret M Condron; George B Benedek; Michael Bowers; David B Teplow
Journal:  J Mol Biol       Date:  2014-04-13       Impact factor: 5.469

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10.  Physicochemical Approach to Understanding the Structure, Conformation, and Activity of Mannan Polysaccharides.

Authors:  Angela Casillo; Antonio Fabozzi; Irene Russo Krauss; Ermenegilda Parrilli; Caroline I Biggs; Matthew I Gibson; Rosa Lanzetta; Marie-Sousai Appavou; Aurel Radulescu; Maria L Tutino; Luigi Paduano; Maria M Corsaro
Journal:  Biomacromolecules       Date:  2021-03-17       Impact factor: 6.988

  10 in total

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