Bykowska K, Wegrzynowicz Z, Lopaciuk S, Kopeć M
Thromb Haemost. 1985 Jun 24;53(3):377-80.
Quantitation of fibronectin (FN) concentration is strongly influenced by FN fragmentation with trypsin, kallikrein and plasmin. Digestion by trypsin and kallikrein leads to a progressive decline in FN detectability by the immunoturbidimetric technique to zero values but is associated with an increase in the height of rockets in the Laurell's electroimmunoassay. Plasmin mediated FN fragmentation induces a strong overestimation of the FN content by the electroimmunoassay and, at very high enzyme concentrations, provokes an underestimation of FN by the immunoturbidimetric technique. The decline in FN reactivity in the immunoturbidimetric assay coincides with the disappearance of heavy fractions migrating only slightly faster than native FN in SDS-PAGE. The increase in the height of rockets in the electroimmunoassay is the highest when fractions of intermediate rate of migration prevail in the SDS-PAGE pattern. Concomitant use of these two immunoassays can distinguish native FN from its degraded form and may possibly provide a partial explanation for discrepancies in published studies on the concentration of circulating FN in various pathological states.
纤连蛋白(FN)浓度的定量受到胰蛋白酶、激肽释放酶和纤溶酶导致的FN片段化的强烈影响。胰蛋白酶和激肽释放酶的消化会使免疫比浊法检测FN的能力逐渐下降至零值,但与Laurell电免疫分析中火箭高度的增加有关。纤溶酶介导的FN片段化会导致电免疫分析对FN含量的严重高估,并且在酶浓度非常高时,会导致免疫比浊法对FN的低估。免疫比浊法中FN反应性的下降与在SDS-PAGE中迁移速度仅略快于天然FN的重链片段的消失相一致。当SDS-PAGE图谱中迁移速率中等的片段占主导时,电免疫分析中火箭高度的增加最为明显。同时使用这两种免疫测定法可以区分天然FN及其降解形式,并可能为各种病理状态下循环FN浓度的已发表研究中的差异提供部分解释。