Beug H, Katz F E, Stein A, Gerisch G
Proc Natl Acad Sci U S A. 1973 Nov;70(11):3150-4. doi: 10.1073/pnas.70.11.3150.
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 x 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.
针对两类靶位点的单价抗体(Fab)可完全阻断盘基网柄菌细胞聚集过程中的细胞间黏附:一类是具有聚集能力的细胞特有的表面结构(“接触位点A”),另一类是生长阶段细胞也存在的表面结构(“接触位点B”)。每个细胞结合3×10⁵个Fab分子足以完全阻断接触位点A,尽管Fab片段覆盖的细胞表面积不超过2%。当使用另一种特异性的Fab片段时,每个细胞可结合高达该值8倍的量,而不影响接触位点A的活性。因此,细胞间黏附的阻断取决于Fab片段与特定靶位点的结合,而不是每个细胞结合的Fab分子总数。这一结论对于归因于接触位点B的细胞黏附也成立。因此,接触位点代表了一类特殊的细胞表面位点,在细胞匀浆以及体内,可通过Fab追踪到它们,并且它们与聚集细胞上存在的大部分细胞表面抗原不同。