Hopman A H, Wiegant J, van Duijn P
Histochemistry. 1986;84(2):169-78. doi: 10.1007/BF00499829.
The mechanisms underlying a new hybridocytochemical method, which is based on mercurated nucleic acid probes and their binding to sulfhydryl-hapten ligands, have been studied. Furthermore we developed a simple procedure for the preparation of mercurated probes at a microgram scale. Nucleic acids immobilized on Sephadex beads have been immunochemically detected after hybridization with mercurated probes and binding of the sulfhydryl-hapten ligand trinitrophenyl-glutathione. In this system, the method proved to be specific and sensitive. However, the same procedure, when applied in situ, failed to give a positive result. ELISA experiments showed that these results cannot be attributed to a suboptimal immunochemical detection of the ligand. Chromatographic analysis of mercurated polynucleotide-ligand complexes revealed, however, an unexpected lability of the mercury-sulfhydryl bond. Under non-equilibrium conditions, as present during a cytochemical washing procedure, the mercury-sulfhydryl b ond was found to dissociate rapidly. On basis of these results the hypothesis was forwarded that the bond between mercurated nucleic acids immobilized on Sephadex and the ligand was stabilized by the positive charge of the Sephadex matrix. This charge was introduced during the cyanogen bromide activation and inactivation necessary for the covalent coupling of nucleic acids to Sephadex. In situ, however, no such positive charges are present. By reversing the charge of the ligand we expected to stabilize the mercury-sulfhydryl bond. In a subsequent paper data are presented that confirm this hypothesis.
对一种基于汞化核酸探针及其与巯基半抗原配体结合的新型杂交细胞化学方法的潜在机制进行了研究。此外,我们开发了一种简单的程序,可在微克规模上制备汞化探针。固定在葡聚糖凝胶珠上的核酸在与汞化探针杂交并结合巯基半抗原配体三硝基苯基谷胱甘肽后,已通过免疫化学方法进行检测。在该系统中,该方法被证明具有特异性和敏感性。然而,同样的程序在原位应用时未能得到阳性结果。酶联免疫吸附测定实验表明,这些结果不能归因于配体免疫化学检测的次优。然而,汞化多核苷酸 - 配体复合物的色谱分析揭示了汞 - 巯基键出人意料的不稳定性。在细胞化学洗涤过程中存在的非平衡条件下,发现汞 - 巯基键迅速解离。基于这些结果,提出了一种假设,即固定在葡聚糖凝胶上的汞化核酸与配体之间的键通过葡聚糖基质的正电荷得以稳定。这种电荷是在核酸与葡聚糖共价偶联所需的溴化氰活化和失活过程中引入的。然而,在原位不存在这种正电荷。通过反转配体的电荷,我们期望稳定汞 - 巯基键。在随后的一篇论文中给出的数据证实了这一假设。