Home LiteratureArticle Details
PMID: 164663 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Fatty acid chain flexibility in the membranes of normal and transformed fibroblasts.

Gaffney BJ

Abstract

Fatty acid spin labels were used to measure the inherent flexibility of the lipid acyl chains in intact cell membranes of 3T3 mouse fibroblasts and several varieties of transformed 3T3 cells. No significant differences in inherent lipid flexibility were detected in the normal and transformed mouse fibroblasts. These results are compared with similar results obtained earlier for chick embryo fibroblasts. For the cells studied, a difference in the mobility of membrane glycoproteins of normal and transformed fibroblasts has either been demonstrated directly or inferred from differential agglutinability by other investigations. Therefore, a basis for correlating glycoprotein mobility and lipid motion in these cells was not found.

MeSH Terms
Animals Avian Sarcoma Viruses Cell Line Cell Membrane Cell Transformation, Neoplastic Chemical Phenomena Chemistry Electron Spin Resonance Spectroscopy Fatty Acids Fibroblasts Mice Spin Labels
Chemicals
Fatty Acids Spin Labels
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Gaffney B J
References (27)
27 references, click to expand
  1. Motion of fatty acid spin labels in the plasma membrane of mycoplasma.
    Biochim Biophys Acta. 1970;219(1):104-13 PMID: 4319690
  2. The interaction of small molecules with spin-labelled erythrocyte membranes.
    Biochim Biophys Acta. 1970 Dec 1;219(2):415-27 PMID: 4322299
  3. Inside-outside transitions of phospholipids in vesicle membranes.
    Biochemistry. 1971 Mar 30;10(7):1111-20 PMID: 4324203
  4. A spin label study of sarcoplasmic vesicles.
    Eur J Biochem. 1971 Jul 15;21(1):17-21 PMID: 4328007
  5. The isolation and characterization of plasma membrane from cultured cells. I. The chemical composition of membrane isolated from uninfected and oncogenic RNA virus-converted chick embryo fibroblasts.
    Biochim Biophys Acta. 1971 Dec 3;249(2):419-34 PMID: 4332411
  6. Agglutination of normal and rous sarcoma virus-transformed chick embryo cells by concanavalin A and wheat germ agglutinin.
    Nat New Biol. 1972 Feb 9;235(58):184-5 PMID: 4334195
  7. The fraction of the lipid in a biological membrane that is in a fluid state: a spin label assay.
    Biochem Biophys Res Commun. 1972 Apr 14;47(1):273-81 PMID: 4337427
  8. Lateral diffusion in spin-labeled phosphatidylcholine multilayers.
    J Am Chem Soc. 1972 Jun 28;94(13):4475-81 PMID: 4338553
  9. Agglutinability by plant lectins increases after RNA virus transformation.
    Virology. 1972 Jul;49(1):339-41 PMID: 4338995
  10. Preparation and properties of phospholipid bilayers containing rhodopsin.
    Proc Natl Acad Sci U S A. 1972 Sep;69(9):2617-21 PMID: 4341702
  11. Changes in acyl group composition of phospholipids from chicken embryonic fibroblasts after transformation by Rous sarcoma virus.
    Biochem Biophys Res Commun. 1972 Oct 6;49(1):114-20 PMID: 4342719
  12. Lipid studies of Rous sarcoma virus and host cell membranes.
    Virology. 1972 Nov;50(2):550-7 PMID: 4344196
  13. The effect of two inhalation anesthetics on the order of spin-labeled phospholipid vesicles.
    Biochim Biophys Acta. 1973 Jan 26;291(2):321-7 PMID: 4347901
  14. Lateral phase separation in phospholipid membranes.
    Biochemistry. 1973 Jun 5;12(12):2351-60 PMID: 4351059
  15. Lateral phase separations in binary mixtures of cholesterol and phospholipids.
    Biochem Biophys Res Commun. 1973 Jul 17;53(2):446-51 PMID: 4352068
  16. A comparative evaluation of the distribution of concanavalin A-binding sites on the surfaces of normal, virally-transformed, and protease-treated fibroblasts.
    Proc Natl Acad Sci U S A. 1973 Jun;70(6):1625-9 PMID: 4352644
  17. Rotational relaxation time of concanavalin A bound to the surface membrane of normal and malignant transformed cells.
    J Mol Biol. 1973 Dec 5;81(2):245-53 PMID: 4360027
  18. The effect of prostaglandins E1 and E2 on the human erythrocyte as monitored by spin labels.
    Biochem Biophys Res Commun. 1974 Jan 23;56(2):478-83 PMID: 4363055
  19. A functional acetylcholine receptor in the human erythrocyte.
    Biochem Biophys Res Commun. 1974 Apr 8;57(3):726-32 PMID: 4363939
  20. Differences in membrane fluidity and structure in contact-inhibited and transformed cells.
    Proc Natl Acad Sci U S A. 1974 May;71(5):1992-4 PMID: 4365580
  21. Lateral phase separations in Escherichia coli membranes.
    Biochim Biophys Acta. 1974 Apr 29;345(2):220-30 PMID: 4366812
  22. Membrane fatty acid replacements and their effect on growth and lectin-induced agglutinability.
    Proc Natl Acad Sci U S A. 1974 Aug;71(8):3115-9 PMID: 4528640
  23. The interactions of lectins with animal cell surfaces.
    Int Rev Cytol. 1974;39:89-190 PMID: 4611947
  24. Lateral diffusion of rhodopsin in the photoreceptor membrane.
    Nature. 1974 Feb 15;247(5441):438-41 PMID: 4818543
  25. Difference in microviscosity induced by different cholesterol levels in the surface membrane lipid layer of normal lymphocytes and malignant lymphoma cells.
    J Mol Biol. 1974 Jan 5;85(4):603-15 PMID: 4851371
  26. Physics and chemistry of spin labels.
    Q Rev Biophys. 1970 Feb;3(1):91-136 PMID: 4908377
  27. Molecular motion in spin-labeled phospholipids and membranes.
    J Am Chem Soc. 1971 Jan 27;93(2):314-26 PMID: 5541516
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1975-02-00
Pages
664-8
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC432375
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: [email protected]