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用于肠道病毒间接免疫荧光和免疫过氧化物酶鉴定的技术及免疫试剂比较

Comparison of techniques and immunoreagents used for indirect immunofluorescence and immunoperoxidase identification of enteroviruses.

作者信息

Herrmann J E, Morse S A, Collins M F

出版信息

Infect Immun. 1974 Jul;10(1):220-6. doi: 10.1128/iai.10.1.220-226.1974.

Abstract

Peroxidase-conjugated antibodies were found to be as sensitive as those conjugated to fluorescein-isothiocyanate (FITC) for identification of selected enterovirus types by the indirect technique. Peroxidase conjugates, however, were found to give fewer nonspecific reactions. The reasons for the higher specificity of the immunoperoxidase technique appear to be related to the relative size, charge, and uniformity of the preparations. Monomers of peroxidase-conjugated globulin are larger than those of FITC conjugates, but the latter readily form aggregates. This was shown by chromatography on Sepharose 6B columns: various FITC-conjugated globulins eluted before those conjugated to peroxidase and before (125)I-labeled immunoglobulin G. The net charge of the conjugates was determined by adsorption to ion-exchange columns. FITC-labeled globulins had a negative net charge, eluting at pH 5.1 from diethylamino-ethyl-Sephadex A-50 columns. Peroxidase conjugates were not retained by either cationic or anionic exchangers at pH values ranging from 4.0 to 10.5. Further, the fluorescein/protein ratios of FITC conjugates from different commercial sources and of those prepared in the laboratory were found to be variable; higher fluorescein/protein ratios (>2:1) give a higher degree of nonspecific reactions, whereas the peroxidase/protein ratio does not appear to affect specificity. These characteristics of peroxidase conjugates make the immunoperoxidase technique easier to standardize and more reliable for enterovirus identification than the immunofluorescence technique.

摘要

已发现过氧化物酶偶联抗体在通过间接技术鉴定特定肠道病毒类型时,与异硫氰酸荧光素(FITC)偶联的抗体一样敏感。然而,发现过氧化物酶偶联物产生的非特异性反应较少。免疫过氧化物酶技术具有更高特异性的原因似乎与制剂的相对大小、电荷和均匀性有关。过氧化物酶偶联球蛋白的单体比FITC偶联物的单体大,但后者容易形成聚集体。这通过在琼脂糖6B柱上的色谱分析得到证明:各种FITC偶联球蛋白在与过氧化物酶偶联的球蛋白之前以及在(125)I标记的免疫球蛋白G之前洗脱。通过吸附到离子交换柱上来测定偶联物的净电荷。FITC标记的球蛋白具有负净电荷,在pH 5.1时从二乙氨基乙基-葡聚糖A-50柱上洗脱。在pH值为4.0至10.5的范围内,过氧化物酶偶联物既不被阳离子交换剂也不被阴离子交换剂保留。此外,发现来自不同商业来源以及实验室制备的FITC偶联物的荧光素/蛋白质比率是可变的;较高的荧光素/蛋白质比率(>2:1)会产生更高程度的非特异性反应,而过氧化物酶/蛋白质比率似乎不影响特异性。过氧化物酶偶联物的这些特性使得免疫过氧化物酶技术比免疫荧光技术更容易标准化,并且在肠道病毒鉴定方面更可靠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93d0/414981/e1ccbcbb830b/iai00247-0236-a.jpg

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