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一种受体结合位点数量减少的霍乱毒素衍生物与培养中的完整细胞之间的相互作用。

Interaction of a cholera toxin derivative containing a reduced number of receptor binding sites with intact cells in culture.

作者信息

De Wolf M J, Dams E, Dierick W S

机构信息

RUCA-Laboratory for Human Biochemistry, University of Antwerp, Belgium.

出版信息

Biochim Biophys Acta. 1994 Sep 8;1223(2):296-305. doi: 10.1016/0167-4889(94)90240-2.

Abstract

Hybrid CTB (hCTB), having only one or two functional binding sites, has been constructed from two chemically inactivated derivatives of CTB. One inactive derivative consisted of CTB formylated in the lone Trp-88 of each beta-chain (fCTB), whereas the other inactive derivative consisted of CTB specifically succinylated in three amino groups located in or near the receptor binding site (sssCTB). hCTB, fCTB and sssCTB were able to reassociate with CTA and form the corresponding holotoxins hCT, fCT and sssCT as measured by gel filtration chromatography. In contrast to fCT and sssCT, hCT could increase the cAMP content of intact Vero cells in a time- and dose-dependent way: concentrations as low as a few nanograms of hCT per milliliter caused a significant increase in the intracellular cAMP level. The maximal cAMP level induced by hCT (1 microgram/ml) was, however, more than 2-fold lower than that elicited by its native counterpart. At saturating ligand concentrations and at 37 degrees C, the lag periods and rates of CT and hCT induced cAMP accumulation were essentially the same. Treatment of Vero and HeLa cells with GM1 did not affect their difference in response to CT and hCT. When Vero cells treated with hCT were incubated for longer periods of time, a further slow accumulation of cAMP occurred until after about 20 h cAMP levels of cells exposed to CT or hCT were essentially the same. In contrast to Vero and HeLa cells, human skin fibroblasts exhibited an almost identical response to CT as well as to hCT. Acidotropic agents such as chloroquine and monensin affected the CT and hCT induced increase in cAMP content of Vero cells, fibroblasts and GM1 treated Hela cells in a similar way. The results are consistent with the view that CT receptor recognition domains are shared between adjacent beta-chains, that pentavalent binding appears not to be essential for cytotoxicity and that in the cell types studied intracellular processing of CT, hCT is involved.

摘要

杂交霍乱毒素B亚单位(hCTB)由霍乱毒素B亚单位(CTB)的两种化学失活衍生物构建而成,仅具有一或两个功能性结合位点。一种失活衍生物是每个β链中唯一的色氨酸-88被甲酰化的CTB(fCTB),而另一种失活衍生物是受体结合位点内或附近的三个氨基被特异性琥珀酰化的CTB(sssCTB)。通过凝胶过滤色谱法测定,hCTB、fCTB和sssCTB能够与霍乱毒素A亚单位(CTA)重新结合并形成相应的全毒素hCT、fCT和sssCT。与fCT和sssCT不同,hCT能够以时间和剂量依赖的方式增加完整非洲绿猴肾细胞(Vero细胞)中的环磷酸腺苷(cAMP)含量:每毫升低至几纳克的hCT浓度就能使细胞内cAMP水平显著升高。然而,hCT(1微克/毫升)诱导的最大cAMP水平比其天然对应物诱导的水平低2倍多。在饱和配体浓度和37摄氏度下,CT和hCT诱导的cAMP积累的延迟期和速率基本相同。用神经节苷脂GM1处理Vero细胞和人宫颈癌细胞(HeLa细胞)并不影响它们对CT和hCT反应的差异。当用hCT处理的Vero细胞孵育更长时间时,cAMP会进一步缓慢积累,直到大约20小时后,暴露于CT或hCT的细胞的cAMP水平基本相同。与Vero细胞和HeLa细胞不同,人皮肤成纤维细胞对CT和hCT表现出几乎相同的反应。诸如氯喹和莫能菌素等亲酸性试剂以类似的方式影响CT和hCT诱导的Vero细胞、成纤维细胞以及用GM1处理的HeLa细胞中cAMP含量的增加。这些结果与以下观点一致:CT受体识别域在相邻的β链之间共享,五价结合似乎对细胞毒性不是必需的,并且在所研究的细胞类型中,CT、hCT的细胞内加工过程参与其中。

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