Home LiteratureArticle Details
PMID: 8369423 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

The relationship of agarose gel structure to the sieving of spheres during agarose gel electrophoresis.

Biophysical journal ·Vol. 65 ·No. 1 ·1993-07-00 ·Pages 138-48

Griess GA, Guiseley KB, Serwer P

Abstract

To understand the organization of fibers in an agarose gel, digitized electron micrographs are used here to determine the frequency distribution of interfiber distance (2Pc) in thin sections of agarose gels. For a preparation of underivatized agarose, a 1.5% gel has a Pc distribution that is indistinguishable from the Pc distribution of a computer-generated, random-fiber gel; the log of the occurrence frequency (F) decreases linearly as a function of Pc. As the agarose concentration decreases below 1.5%, the semilogarithmic F versus Pc plot becomes progressively less linear. Two straight lines represent the data; the plot is steeper at the lower Pc values. As the percentage of agarose increases above 1.5%, the semilogarithmic F versus Pc plot becomes steeper at the higher Pc values. This change in the shape of semilogarithmic F versus Pc plots is possibly explained by the existence in agarose gels of two zones, one whose Pc distribution is more sensitive to the average agarose concentration than the other. To compare the structure of agarose gels to their sieving during electrophoresis, the root mean square value of Pc (Pc) is compared to the sieving-based radius of the effective pore (PE; Griess et. al. (16)) for both underivatized agarose and a derivatized agarose that has a smaller PE at any given agarose percentage. For 0.8-2.0% gels of either underivatized or derivatized agarose, PE/Pc is a constant within experimental error. Deviations from this constant are observed at lower gel percentages. This relationship of PE to Pc constrains theoretical descriptions of the motion of spheres in fibrous networks.

MeSH Terms
Biophysical Phenomena Biophysics DNA/chemistry,isolation & purification Electrophoresis, Agar Gel Gels/chemistry Microscopy, Electron Particle Size Polymers/chemistry,isolation & purification Sepharose/chemistry
Chemicals
Gels Polymers DNA Sepharose
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Griess G A
Department of Biochemistry, University of Texas Health Sciences Center 78284-7760.
Guiseley K B
Serwer P
References (19)
19 references, click to expand
  1. Problems and prospects in the theory of gel electrophoresis of DNA.
    Q Rev Biophys. 1992 May;25(2):171-204 PMID: 1518924
  2. A study of electrophoretic mobility of DNA in agarose and polyacrylamide gels.
    J Mol Biol. 1991 Oct 5;221(3):981-1005 PMID: 1942040
  3. Determination of the thickness of electron microscopy sections.
    J Ultrastruct Res. 1960 Dec;4:413-9 PMID: 13788121
  4. The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.
    J Cell Biol. 1963 Apr;17:208-12 PMID: 13986422
  5. Tertiary and quaternary structure in aqueous polysaccharide systems which model cell wall cohesion: reversible changes in conformation and association of agarose, carrageenan and galactomannans.
    J Mol Biol. 1972 Jul 14;68(1):153-72 PMID: 5050360
  6. The agarose double helix and its function in agarose gel structure.
    J Mol Biol. 1974 Dec 5;90(2):269-84 PMID: 4453017
  7. Ultrastructure of beaded agarose.
    Arch Biochem Biophys. 1975 Dec;171(2):673-7 PMID: 1200645
  8. Theory of edge detection.
    Proc R Soc Lond B Biol Sci. 1980 Feb 29;207(1167):187-217 PMID: 6102765
  9. Study of agarose gels by electron microscopy of freeze-fractured surfaces.
    Biopolymers. 1982 Sep;21(9):1909-26 PMID: 7126760
  10. Comparison of the physical properties and assembly pathways of the related bacteriophages T7, T3 and phi II.
    J Mol Biol. 1983 Oct 25;170(2):447-69 PMID: 6631966
  11. A rapid method of staining ultrathin sections for surgical pathology TEM with the use of the microwave oven.
    Am J Clin Pathol. 1985 May;83(5):639-41 PMID: 2581442
  12. Use of gel electrophoresis to characterize multimolecular aggregates.
    Methods Enzymol. 1986;130:116-32 PMID: 3773730
  13. Pulsed-field gel electrophoresis of very large DNA molecules.
    Annu Rev Biophys Biophys Chem. 1988;17:287-304 PMID: 3293589
  14. Edge detection in images using Marr-Hildreth filtering techniques.
    J Neurosci Methods. 1988 Nov;26(1):75-81 PMID: 3199849
  15. The sieving of spheres during agarose gel electrophoresis: quantitation and modeling.
    Biopolymers. 1989 Aug;28(8):1475-84 PMID: 2752101
  16. Use of image analysis to quantitate changes in form of mitochondrial DNA after x-irradiation.
    Appl Theor Electrophor. 1989;1(3):163-7 PMID: 2488599
  17. Sieving by agarose gels and its use during pulsed-field electrophoresis.
    Biotechnol Genet Eng Rev. 1990;8:319-43 PMID: 2094274
  18. Microscopic behaviour of DNA during electrophoresis: electrophoretic orientation.
    Q Rev Biophys. 1991 May;24(2):103-64 PMID: 1924681
  19. Thin sections. I. A study of section thickness and physical distortion produced during microtomy.
    J Biophys Biochem Cytol. 1958 May 25;4(3):233-42 PMID: 13549493
Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
0006-3495
Published
1993-07-00
Pages
138-48
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC1225709
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com