Coleman P S, Ewell A J, Good R A
Proc Natl Acad Sci U S A. 1978 Aug;75(8):3766-70. doi: 10.1073/pnas.75.8.3766.
The covalently binding fluorescent probe 5-dimethylamino-1-naphthalenesulfonyl (dansyl) chloride was affixed directly to the plasma membrane of viable human peripheral blood lymphocytes via a solid phase transfer method utilizing Sephadex G-10 as the transfer vehicle. After dansylation, lymphocytes retain maximal short-term viability. Dansyl, as the protein conjugate or as the free acid, does not appear to penetrate the cells to any significant extent. Dansylated mixed lymphocyte cultures respond to lectin mitogen stimulation for at least 72 hr. Furthermore, differential response of dansylated lymphocytes in culture to three plant lectin mitogens provides a clue to the binding loci of concanavalin A with respect to phytohemagglutinin and pokeweed mitogen on the lymphocyte surface receptors for these lectins. The ability to sustain functionally responsive dansylated lymphocytes for several days in culture suggest that such probe-tagged cells may be useful in elucidating aspects of the plasma membrane in the regulation of cell behavior.
通过利用葡聚糖凝胶G - 10作为转移载体的固相转移方法,将共价结合的荧光探针5 - 二甲基氨基 - 1 - 萘磺酰氯(丹磺酰氯)直接附着于有活力的人外周血淋巴细胞的质膜上。丹磺酰化后,淋巴细胞保持最大的短期活力。丹磺酰基作为蛋白质共轭物或游离酸,似乎不会在任何显著程度上穿透细胞。丹磺酰化的混合淋巴细胞培养物对凝集素丝裂原刺激至少有72小时的反应。此外,培养的丹磺酰化淋巴细胞对三种植物凝集素丝裂原的差异反应为伴刀豆球蛋白A相对于植物血凝素和商陆丝裂原在这些凝集素的淋巴细胞表面受体上的结合位点提供了线索。在培养中维持功能反应性丹磺酰化淋巴细胞数天的能力表明,这种探针标记的细胞可能有助于阐明质膜在调节细胞行为方面的作用。