多发性骨髓瘤
体内分布
化学
流式细胞术
癌症研究
体内
肽
多塔
医学
内科学
体外
免疫学
生物化学
生物
有机化学
螯合作用
生物技术
作者
Lele Song,Sujun Jiang,Qi Yang,Wenpeng Huang,Yongkang Qiu,Zhao Chen,Xinyao Sun,Tianyao Wang,Sitong Wu,Yong-Shou Chen,Huajie Zeng,Zihua Wang,Lei Kang
标识
DOI:10.1021/acs.jmedchem.4c00759
摘要
B-cell maturation antigen (BCMA) has emerged as a promising tumor marker for the diagnosis and treatment of multiple myeloma. The noninvasive and rapid detection of BCMA expression in vivo provides significant value in screening and evaluating multiple myeloma patients receiving BCMA-targeted therapy. We identified the BCMA-targeting peptide BP1 from a one-bead-one-compound (OBOC) peptide library using a high-throughput microarray strategy. The BCMA-targeting specificity and affinity of BP1 were assessed by surface plasmon resonance imaging (SPRi), flow cytometry, and confocal imaging. BCMA-positive (H929) and BCMA-negative (K562) subcutaneous tumor models were established and labeled with 68Ga for BP1, followed by PET imaging and biodistribution studies. PET imaging demonstrated that 68Ga-labeled BP1 has significant specific uptake in multiple myeloma, enabling rapid identification of BCMA expression and precise delineation of the disease. Thus, BP1 represents an ideal candidate for multiple myeloma imaging.
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