Thonar E J, Feist S B, Fassbender K, Lenz M E, Matijevitch B L, Kuettner K E
Department of Biochemistry, Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL 60612-3864.
Connect Tissue Res. 1988;17(3):181-97. doi: 10.3109/03008208809015029.
We have developed an enzyme-linked immunosorbent assay (ELISA) with an inhibition step to quantify hen egg white lysozyme (HEWL) on a weight basis. The assay is relatively insensitive to changes in ionic strength or pH. Quantification is not affected by the presence or large amounts of mammalian lysozymes or inhibitors of enzymatic activity such as soluble chitin oligomers. We used this ELISA to show that the HEWL content of chick cartilages increases progressively between days 14 and 18 of embryonic life. The maturation-related increase does not appear to be the result of increased synthesis by the chondrocytes for the latter did not synthesize detectable amounts of lysozyme in vitro. Evidence was obtained to suggest that most, if not all, the lysozyme in cartilage is derived from the surrounding fluids which come in contact with the matrix.
我们开发了一种带有抑制步骤的酶联免疫吸附测定法(ELISA),用于以重量为基础定量测定鸡蛋清溶菌酶(HEWL)。该测定法对离子强度或pH值的变化相对不敏感。定量不受哺乳动物溶菌酶的存在或大量存在以及酶活性抑制剂(如可溶性几丁质低聚物)的影响。我们使用这种ELISA来表明,在胚胎期第14天至18天之间,雏鸡软骨中的HEWL含量逐渐增加。与成熟相关的增加似乎不是软骨细胞合成增加的结果,因为后者在体外并未合成可检测量的溶菌酶。有证据表明,软骨中大部分(如果不是全部)溶菌酶来自与基质接触的周围液体。