» Articles » PMID: 14381423

Electron Densitometry of Stained Virus Particles

Overview
Specialty Cell Biology
Date 1955 Jan 1
PMID 14381423
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Methods are described for determining the relative mass of particles in electron microscope specimens through the measurement of photographic densities in recorded images. These methods were applied to a quantitative study of the amounts of electron stains that could be associated with the particles of tomato bushy stunt virus (BSV) and tobacco mosaic virus (TMV). In the pH range above 2 where the viruses are stable, the amount of stain absorbed is too small to produce adequate contrast in the electron microscope. Maximum stain absorption was achieved at pH about 1 where with several reagents and combinations of reagents the mass of BSV could be increased to about four times that of the unstained particles. Optimum results were obtained with phosphotungstic acid alone or in combination with Pt, Th, or La ions. Since the pH conditions for high stain absorption are normally destructive, morphology is satisfactorily preserved only when the phosphotungstic acid is applied in concentrations of 10 per cent or greater or when the use of destructive reagents is preceded by a preliminary fixation under mild conditions. Maximum staining of TMV increased the mass of the particles to about two times that of the unstained. Estimates of the mass of heavily stained BSV particles indicate that their density is 3.3 gm./cm.(3) The high internal hydration of BSV probably accounts for the greater stain absorption and penetration compared to those of TMV which has very low or zero internal hydration. Anomalous images resulting from the use of electron stains are shown and discussed.

Citing Articles

Machine learning for cross-scale microscopy of viruses.

Petkidis A, Andriasyan V, Greber U Cell Rep Methods. 2023; 3(9):100557.

PMID: 37751685 PMC: 10545915. DOI: 10.1016/j.crmeth.2023.100557.


Biophysical Screening Pipeline for Cryo-EM Grid Preparation of Membrane Proteins.

Niebling S, Veith K, Vollmer B, Lizarrondo J, Burastero O, Schiller J Front Mol Biosci. 2022; 9:882288.

PMID: 35813810 PMC: 9259969. DOI: 10.3389/fmolb.2022.882288.


IgG Antibody 3D Structures and Dynamics.

Jay J, Bray B, Qi Y, Igbinigie E, Wu H, Li J Antibodies (Basel). 2019; 7(2).

PMID: 31544870 PMC: 6698877. DOI: 10.3390/antib7020018.


Sad State of Phage Electron Microscopy. Please Shoot the Messenger.

Ackermann H Microorganisms. 2016; 2(1):1-10.

PMID: 27694773 PMC: 5029504. DOI: 10.3390/microorganisms2010001.


Cryo-electron tomography of bacterial viruses.

Guerrero-Ferreira R, Wright E Virology. 2012; 435(1):179-86.

PMID: 23217626 PMC: 5119483. DOI: 10.1016/j.virol.2012.08.022.


References
1.
KAHLER H, LLOYD Jr B . Electron microscopic study of the Shope papilloma virus. J Natl Cancer Inst. 1952; 12(6):1167-75. View

2.
LEONARD Jr B, Anderegg J, Shulman S, Kaesberg P, BEEMAN W . An x-ray investigation of the sizes and hydrations of three spherical virus macromolecules in solution. Biochim Biophys Acta. 1953; 12(4):499-507. DOI: 10.1016/0006-3002(53)90180-2. View