Mukoyama M, Nakao K, Sugawa H, Morii N, Sugawara A, Yamada T, Itoh H, Shiono S, Saito Y, Arai H
Department of Medicine, Kyoto University School of Medicine, Japan.
Hypertension. 1988 Aug;12(2):117-21. doi: 10.1161/01.hyp.12.2.117.
A monoclonal antibody to alpha-human atrial natriuretic polypeptide (alpha-hANP), KY-ANP-I, has been produced by fusion of a nonproducing mouse myeloma cell line, X63-Ag8.653, with spleen cells from BALB/c mice immunized with synthetic alpha-hANP conjugated to bovine thyroglobulin using the carbodiimide coupling procedure. Hybridomas were screened for antibody production by radioimmunoassay using culture media and 125I-alpha-hANP. They were cloned by the limiting dilution technique, expanded in culture, and injected intraperitoneally into BALB/c mice. The obtained antibody belonged to the immunoglobulin G1 subclass. Analysis by a Scatchard plot revealed a high affinity for alpha-hANP, with an association constant of 3.1 x 10(10) M-1. With this monoclonal antibody, a specific radioimmunoassay for alpha-hANP has been established. The antibody in mouse ascites was available for radioimmunoassay at a final dilution of 1:10(6). Values of IC10 and IC50 in this radioimmunoassay were 3 and 30 fmol/tube, respectively. The radioimmunoassay showed a cross-reactivity of 0.9% with alpha-rat ANP. alpha-hANP-(8-22) and alpha-ANP-(1-6) exhibited less cross-reactivity than alpha-rat ANP on a molar basis. There was no cross-reaction with alpha-ANP-(17-28). Thus, the recognized epitope must be located in the N-terminal half of the ring structure of alpha-hANP including Met12 residue. This radioimmunoassay could detect gamma-hANP and beta-hANP as well as alpha-hANP. The monoclonal antibody was also useful for immunohistochemical studies. ANP-positive cells were finely stained in the human atrium using the avidin-biotin-peroxidase complex technique.(ABSTRACT TRUNCATED AT 250 WORDS)
一种针对α-人心房利钠多肽(α-hANP)的单克隆抗体KY-ANP-I,是通过将不产生抗体的小鼠骨髓瘤细胞系X63-Ag8.653与用碳二亚胺偶联法将合成的α-hANP与牛甲状腺球蛋白偶联免疫的BALB/c小鼠的脾细胞融合产生的。使用培养基和125I-α-hANP通过放射免疫测定法筛选杂交瘤的抗体产生情况。通过有限稀释技术对它们进行克隆,在培养中扩增,并腹腔注射到BALB/c小鼠体内。获得的抗体属于免疫球蛋白G1亚类。通过Scatchard图分析显示对α-hANP具有高亲和力,缔合常数为3.1×10(10) M-1。利用这种单克隆抗体,建立了一种针对α-hANP的特异性放射免疫测定法。小鼠腹水中的抗体在最终稀释度为1:10(6)时可用于放射免疫测定。该放射免疫测定法中IC10和IC50的值分别为3和30 fmol/管。该放射免疫测定法显示与α-大鼠ANP的交叉反应性为0.9%。α-hANP-(8-22)和α-ANP-(1-6)在摩尔基础上的交叉反应性比α-大鼠ANP低。与α-ANP-(17-28)无交叉反应。因此,识别的表位必须位于α-hANP环结构的N端一半,包括Met12残基。这种放射免疫测定法可以检测γ-hANP、β-hANP以及α-hANP。该单克隆抗体也可用于免疫组织化学研究。使用抗生物素蛋白-生物素-过氧化物酶复合物技术,在人的心房中ANP阳性细胞被精细染色。(摘要截短于250字)