Literature DB >> 18237650

Mass mapping of large globin complexes by scanning transmission electron microscopy.

Joseph S Wall1, Martha N Simon, Beth Y Lin, Serge N Vinogradov.   

Abstract

Scanning transmission electron microscopy (STEM) of unstained, freeze-dried biological macromolecules in the dark-field mode provides an image based on the number of electrons elastically scattered by the constituent atoms of the macromolecule. The image of each isolated particle provides information about the projected structure of the latter, and its integrated intensity is directly related to the mass of the selected particle. Particle images can be sorted by shape, providing independent histograms of mass to study assembly/disassembly intermediates. STEM is optimized for low-dose imaging and is suitable for accurate measurement of particle masses over the range from about 30 kDa to 1,000 MDa. This article describes the details of the method developed at the Brookhaven National Laboratory STEM facility and illustrates its application to the mass mapping of large globin complexes.

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Year:  2008        PMID: 18237650     DOI: 10.1016/S0076-6879(08)36027-3

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  8 in total

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2.  Conformational switching in PolyGln amyloid fibrils resulting from a single amino acid insertion.

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3.  Helical filaments of human Dmc1 protein on single-stranded DNA: a cautionary tale.

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Journal:  J Mol Biol       Date:  2010-06-30       Impact factor: 5.469

4.  Structure and function of the adhesive type IV pilus of Sulfolobus acidocaldarius.

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5.  α-Synuclein Amyloid Fibrils with Two Entwined, Asymmetrically Associated Protofibrils.

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Journal:  J Biol Chem       Date:  2015-12-07       Impact factor: 5.157

6.  Cryoelectron microscopy structure of purified gamma-secretase at 12 A resolution.

Authors:  Pamela Osenkowski; Hua Li; Wenjuan Ye; Dongyang Li; Lorene Aeschbach; Patrick C Fraering; Michael S Wolfe; Dennis J Selkoe; Huilin Li
Journal:  J Mol Biol       Date:  2008-11-05       Impact factor: 5.469

7.  α-Synuclein occurs physiologically as a helically folded tetramer that resists aggregation.

Authors:  Tim Bartels; Joanna G Choi; Dennis J Selkoe
Journal:  Nature       Date:  2011-08-14       Impact factor: 49.962

8.  Three-dimensional reconstruction of the Shigella T3SS transmembrane regions reveals 12-fold symmetry and novel features throughout.

Authors:  Julie L Hodgkinson; Ashley Horsley; David Stabat; Martha Simon; Steven Johnson; Paula C A da Fonseca; Edward P Morris; Joseph S Wall; Susan M Lea; Ariel J Blocker
Journal:  Nat Struct Mol Biol       Date:  2009-04-26       Impact factor: 15.369

  8 in total

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