Crossref journal-article
Proceedings of the National Academy of Sciences
Proceedings of the National Academy of Sciences (341)
Abstract

Cell-to-cell adhesion during aggregation of Dictyostelium discoideum cells is completely blocked by univalent antibody (Fab) directed against two classes of target sites: surface structures characteristic for aggregation-competent cells (“contact sites A”) and others present also on growth-phase cells (“contact sites B”). 3 × 10 5 Fab molecules bound per cell are sufficient to block contact sites A completely, although the Fab fragments cover not more than 2% of the total cell surface. Up to 8-fold this value can be bound per cell when Fab fragments of another specificity are used, without affecting activity of contact sites A. Blockage of cell-to-cell adhesion therefore depends on the binding of Fab fragments to specific target sites, rather than on the total number of Fab molecules bound per cell. This conclusion is also valid for cell adhesion attributed to contact sites B. Contact sites therefore represent a special class of cell-surface sites which, in cell homogenates as well as in vivo , can be traced by Fab, and which are not identical with the bulk of cell-surface antigens present on aggregating cells.

Bibliography

Beug, H., Katz, F. E., Stein, A., & Gerisch, G. (1973). Quantitation of Membrane Sites in Aggregating Dictyostelium Cells by Use of Tritiated Univalent Antibody. Proceedings of the National Academy of Sciences, 70(11), 3150–3154.

Authors 4
  1. H. Beug (first)
  2. F. E. Katz (additional)
  3. A. Stein (additional)
  4. G. Gerisch (additional)
References 0 Referenced 59

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Dates
Type When
Created 19 years, 2 months ago (May 31, 2006, 2:37 a.m.)
Deposited 3 years, 4 months ago (April 13, 2022, 10:32 a.m.)
Indexed 1 year, 6 months ago (Feb. 23, 2024, 1:24 p.m.)
Issued 51 years, 9 months ago (Nov. 1, 1973)
Published 51 years, 9 months ago (Nov. 1, 1973)
Published Online 51 years, 9 months ago (Nov. 1, 1973)
Published Print 51 years, 9 months ago (Nov. 1, 1973)
Funders 0

None