Recombinant Proteins Department, Breast Cancer Research Center, Motamed Cancer Institute, ACECR, Tehran, Iran.
Department of Research and Development, Sharif Ultra High Nanotechnologists (SUN) Company, Tehran, Iran.
Mol Biol Rep. 2020 Jan;47(1):225-234. doi: 10.1007/s11033-019-05122-w. Epub 2019 Oct 22.
Leukemic cancer stem cells (LSCs), aberrantly overexpressing CD45RA are among the major causes of relapse following chemotherapy in patients with acute myeloid leukemia and serve as a highly sensitive marker for predicting relapse occurrence following chemotherapy. The main purpose of current study was to develop a sensitive approach for detecting LSCs based on a conjugate of an anti-CD45 scFv and quantum dot. The variable light and heavy chain sequences of a recently developed anti-CD45RA monoclonal antibody were derived from hybridoma cells and PCR amplified to construct scFv. Following insertion of scFv gene into a pET32a-lic vector and expression in Escherichia coli and purification, the purified scFv, was conjugated with carbon dots (C dots) and used for the detection of CD45RA cells while CD45RA-cells served as negative control. Subsequently, Functional activity of the conjugate was analyzed by flow cytometry and ICC to detect the cell surface antigen binding and detection ability. Based on results, purified CD45RA scFv conjugated C dots could specifically recognize CD45RA positive cells, but not any CD45RA negative ones. In conclusion, here we developed a low-cost but very efficient approach for detection of CD45RA positive cells including LSCs.
白血病癌症干细胞 (LSCs) 异常过表达 CD45RA,是急性髓系白血病患者化疗后复发的主要原因之一,并且可作为预测化疗后复发发生的高度敏感标志物。本研究的主要目的是基于抗 CD45 scFv 和量子点的缀合物开发一种用于检测 LSCs 的敏感方法。最近开发的抗 CD45RA 单克隆抗体的可变轻链和重链序列来自杂交瘤细胞,并通过 PCR 扩增来构建 scFv。将 scFv 基因插入 pET32a-lic 载体并在大肠杆菌中表达和纯化后,将纯化的 scFv 与碳点 (C 点) 缀合,并用于检测 CD45RA 细胞,而 CD45RA 细胞则作为阴性对照。随后,通过流式细胞术和 ICC 分析缀合物的功能活性,以检测细胞表面抗原结合和检测能力。基于结果,纯化的 CD45RA scFv 缀合的 C 点可以特异性识别 CD45RA 阳性细胞,但不能识别任何 CD45RA 阴性细胞。总之,我们在这里开发了一种低成本但非常有效的方法来检测包括 LSCs 在内的 CD45RA 阳性细胞。