Scanning probe microscopy studies of cereal seed storage protein structures

Arthur S. Tatham*, Neil H. Thomson, Terence J. McMaster, Andrew D.L. Humphris, Mervyn J. Miles, Peter R. Shewry

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

Abstract

Scanning probe microscopes (SPMs) share a number of common features which give the techniques advantages over conventional light and electron microscopy. First, high resolution, up to the atomic level, is possible in certain cases, and second, they are nondestructive, requiring no staining or coating and the images can be obtained in the hydrated state or under water. Scanning probe microscopes, particularly scanning tunnelling microscopes (STM) and atomic force microscopes (AFM), have been used to study food- related systems, ranging from relatively large structures such as starch granules to the organisation of secondary structures in proteins and the interaction of proteins. The seed storage proteins (gluten) of wheat are responsible for the viscous and elastic properties of wheat doughs that allow them to be used for a wide range of different food products. Using AFM and STM, images of individual and groups of proteins have been obtained in both the dry and hydrated states. The ability to work in liquid environments allows the conformation of proteins to be determined under conditions approaching 'native'. The AFM and STM have been used to image both gliadins and glutenins and to study their aggregative behaviour in relation to gluten and dough systems.

Original languageEnglish
Pages (from-to)293-298
Number of pages6
JournalScanning
Volume21
Issue number5
DOIs
Publication statusPublished - 1999
Externally publishedYes

Keywords

  • Atomic force microscopy
  • Gliadins
  • Gluten
  • Glutenins
  • Prolamins
  • Scanning probe microscopes
  • Scanning tunnelling microscopy

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