Szöllösi J, Damjanovich S, Goldman C K, Fulwyler M J, Aszalos A A, Goldstein G, Rao P, Talle M A, Waldmann T A
Department of Biophysics, Medical University School of Debrecen, Hungary.
Proc Natl Acad Sci U S A. 1987 Oct;84(20):7246-50. doi: 10.1073/pnas.84.20.7246.
Two monoclonal antibodies (OKT27 and OKT27b) have been produced that react with distinct epitopes of a 95-kDa peptide. The T27 antigen is widely distributed, being expressed on B lymphocytes, monocytes, and adult T-leukemic cells but not on polymorphonuclear leukocytes or platelets. There was a low level of T27 expression on resting T cells that increased on T-cell activation. In preliminary studies, the OKT27b antibody coprecipitated a 55-kDa peptide, as well as the 95-kDa peptide, from the radiolabeled cells of the HuT 102B2 cell line. Preclearance with anti-Tac, a monoclonal antibody to the 55-kDa peptide of the multichain interleukin 2 receptor, removed the 55-kDa but not the 95-kDa peptide from subsequent OKT27b immunoprecipitates of HuT 102B2 extracts, suggesting the possibility that the T27 peptide was associated with the Tac peptide. However, the precipitation of the p55 Tac peptide by OKT27b was quite inconsistent. Thus, additional information was sought using a flow cytometric energy transfer technique to provide a physical estimation of the proximity between the Tac and the T27 peptides. The flow cytometric version of the fluorescence resonance energy transfer technique permits the determination of inter- and intramolecular distances at 2- to 10-nm levels on a cell-by-cell basis. Using this approach, there was a mean energy transfer of 7.3% with HuT 102B2 cells when fluorescein isothiocyanate anti-Tac served as the donor and tetramethylrhodamine isothiocyanate OKT27 served as the acceptor. In contrast, there was no energy transfer in comparable studies observed when fluorescein anti-Tac and rhodamine anti-transferrin receptor antibodies were used. These observations support the conclusion that there is a close nonrandom proximity in HuT 102B2 cells between the 95-kDa peptide identified by the OKT27 monoclonal antibody and the p55 Tac peptide of the multichain interleukin 2 receptor.
已产生两种单克隆抗体(OKT27和OKT27b),它们与一种95 kDa肽的不同表位发生反应。T27抗原广泛分布,在B淋巴细胞、单核细胞和成人T白血病细胞上表达,但在多形核白细胞或血小板上不表达。静息T细胞上T27表达水平较低,在T细胞活化时会升高。在初步研究中,OKT27b抗体从HuT 102B2细胞系的放射性标记细胞中共同沉淀出一种55 kDa肽以及95 kDa肽。用抗Tac(一种针对多链白细胞介素2受体55 kDa肽的单克隆抗体)进行预清除,从HuT 102B2提取物随后的OKT27b免疫沉淀中去除了55 kDa肽但未去除95 kDa肽,这表明T27肽可能与Tac肽相关。然而,OKT27b对p55 Tac肽的沉淀相当不稳定。因此,使用流式细胞术能量转移技术来寻求更多信息,以对Tac肽和T27肽之间的接近程度进行物理评估。荧光共振能量转移技术的流式细胞术版本允许在逐个细胞的基础上测定2至10纳米水平的分子间和分子内距离。使用这种方法,当异硫氰酸荧光素抗Tac作为供体且异硫氰酸四甲基罗丹明OKT27作为受体时,HuT 102B2细胞的平均能量转移为7.3%。相比之下,当使用荧光素抗Tac和罗丹明抗转铁蛋白受体抗体进行类似研究时,未观察到能量转移。这些观察结果支持以下结论:在HuT 102B2细胞中,由OKT27单克隆抗体识别的95 kDa肽与多链白细胞介素2受体的p55 Tac肽之间存在紧密的非随机接近关系。