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[基于单克隆抗体的夹心酶免疫分析法检测溶杆菌属XL1菌株的AlpA和AlpB溶菌性内肽酶前肽]

[Detection of AlpA and AlpB lytic endopeptidase propeptides of Lysobacter sp. XL1 by sandwich-enzyme immunoassay based on monoclonal antibodies].

作者信息

Rudenko N V, Tsfasman I M, Latypov O R, Ledova L A, Krasovskaia L A, Karatovskaia A P, Brovko F A, Vasil'eva N V, Stepnaia O A

出版信息

Bioorg Khim. 2014 May-Jun;40(3):297-304. doi: 10.1134/s1068162014030133.

Abstract

The extracellular lytic endopeptidases AlpA and AlpB of the bacterium Lysobacter sp. XL1 are highly homologous and synthesized as precursors consisting of signal peptide, propeptide and mature form. In this work, two monoclonal antibodies against propeptide endopeptidase AlpA (ProA) and eleven against propeptide endopeptidase AlpB (ProB) were obtained to study the AlpA and AlpB endopeptidases secretion. The affinity constants of the antibodies against ProA were 2.9 x 10(9) and 3.5 x 10(9) M(-1), and the affinity constants of the antibodies against ProB were from 1.5 x 10(8) to 2.2 x 10(9) M(-1). The obtained antibodies did not have cross-reactivity between themselves, as well as mature forms of the enzymes. The monoclonal antibodies based sandwich-type enzyme immunoassay has been developed for measuring the propeptide in a native form. The linear range of determination ProA was 1.5-100 ng/mL with 6% error of measurement, and for determining ProB 0.2-6.25 ng/mL with 6% error. Using the developed assay, ProA and ProB propeptides have been detected in cell lysates of Lysobacter sp. XL1 in an amount 1.18 ± 0.03 ng and 0.096 ± 0.002 ng per 1 OD540 of the bacterial culture, respectively. The immunochemical assay for detection various forms of AlpA and AlpB lytic endopeptidases can be useful when dealing with issues related to their secretion into the environment.

摘要

溶杆菌属XL1菌株的细胞外裂解性内肽酶AlpA和AlpB高度同源,以前体形式合成,前体由信号肽、前肽和成熟形式组成。在本研究中,获得了两种抗前肽内肽酶AlpA(ProA)的单克隆抗体和十一种抗前肽内肽酶AlpB(ProB)的单克隆抗体,用于研究AlpA和AlpB内肽酶的分泌情况。抗ProA抗体的亲和常数分别为2.9×10⁹和3.5×10⁹ M⁻¹,抗ProB抗体的亲和常数为1.5×10⁸至2.2×10⁹ M⁻¹。所获得的抗体之间以及与酶的成熟形式均无交叉反应。已开发出基于单克隆抗体的夹心型酶免疫测定法,用于检测天然形式的前肽。测定ProA的线性范围为1.5 - 100 ng/mL,测量误差为6%,测定ProB的线性范围为0.2 - 6.25 ng/mL,测量误差为6%。使用所开发的测定法,在溶杆菌属XL1菌株的细胞裂解物中检测到ProA和ProB前肽,每1 OD540细菌培养物中分别为1.18±0.03 ng和0.096±0.002 ng。当处理与AlpA和AlpB裂解性内肽酶分泌到环境中相关的问题时,用于检测其各种形式的免疫化学测定法可能会很有用。

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