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抗小鼠脑钠肽(BNP)单克隆抗体的制备及BNP在小鼠体内的组织分布

Preparation of a monoclonal antibody against mouse brain natriuretic peptide (BNP) and tissue distribution of BNP in mice.

作者信息

Nakagawa M, Tanaka I, Suga S, Ogawa Y, Tamura N, Goto M, Sugawara A, Yoshimasa T, Itoh H, Mukoyama M

机构信息

Department of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Japan.

出版信息

Clin Exp Pharmacol Physiol Suppl. 1995 Dec;22(1):S186-7. doi: 10.1111/j.1440-1681.1995.tb02874.x.

Abstract
  1. In order to explore the significance of brain natriuretic peptide (BNP), a cardiac hormone secreted from the ventricle, in mice, we prepared a monoclonal antibody against mouse BNP (mBNP) and established a specific radioimmunoassay (RIA) for mBNP. 2. A monoclonal antibody, KY-mBNP-I, was prepared by the fusion of mouse myeloma cells X63-Ag8.653 with spleen cells of the BALB/c mouse immunized with synthetic mBNP[108-121] conjugated to bovine thyroglobulin. KY-mBNP-I belonged to an IgG2a subclass and showed a high affinity for mBNP (Ka = 1.8 x 10(11) mol/L-1). 3. The RIA established that using KY-mBNP-I was highly sensitive and specific for mBNP, with an IC50 value of 3 fmol/tube and cross-reactivities of less than 0.003% with related natriuretic peptides. mBNP-like immunoreactivity (mBNP-LI) was detected in the mouse atrium (0.35 +/- 0.02 nmol/g), ventricle (20.5 +/- 0.5 pmol/g) and kidney (0.50 +/- 0.05 pmol/g), but not in other tissues including brain. 4. Gel filtration analysis revealed that the major component of tissue mBNP-LI was co-eluted with synthetic mBNP[77-121], a 45-amino acid mature peptide. 5. The monoclonal antibody and RIA for mBNP established here will provide useful tools to investigate the functional significance of BNP in mice, coupled with the genetic engineering approach.
摘要
  1. 为了探究心室分泌的心脏激素脑钠肽(BNP)在小鼠体内的意义,我们制备了抗小鼠BNP(mBNP)的单克隆抗体,并建立了mBNP的特异性放射免疫测定法(RIA)。2. 通过将小鼠骨髓瘤细胞X63-Ag8.653与用与牛甲状腺球蛋白偶联的合成mBNP[108-121]免疫的BALB/c小鼠的脾细胞融合,制备了单克隆抗体KY-mBNP-I。KY-mBNP-I属于IgG2a亚类,对mBNP具有高亲和力(Ka = 1.8 x 10(11) mol/L-1)。3. 建立的使用KY-mBNP-I的RIA对mBNP具有高度敏感性和特异性,IC50值为3 fmol/管,与相关利钠肽的交叉反应性小于0.003%。在小鼠心房(0.35 +/- 0.02 nmol/g)、心室(20.5 +/- 0.5 pmol/g)和肾脏(0.50 +/- 0.05 pmol/g)中检测到mBNP样免疫反应性(mBNP-LI),但在包括脑在内的其他组织中未检测到。4. 凝胶过滤分析显示,组织mBNP-LI的主要成分与合成的mBNP[77-121](一种45个氨基酸的成熟肽)共洗脱。5. 这里建立的mBNP单克隆抗体和RIA将为结合基因工程方法研究BNP在小鼠体内的功能意义提供有用的工具。

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