Department of Biomedical Polymers, Institute of Macromolecular Chemistry CAS, Heyrovského nám. 2, Prague, 162 00, Czech Republic.
CLIP (Childhood Leukemia Investigation Prague), Department of Paediatric Haematology and Oncology, Second Faculty of Medicine, Charles University and University Hospital Motol, V Úvalu 84, Prague, 150 06, Czech Republic.
Macromol Biosci. 2024 Feb;24(2):e2300306. doi: 10.1002/mabi.202300306. Epub 2023 Sep 24.
Herein, an advanced bioconjugation technique to synthesize hybrid polymer-antibody nanoprobes tailored for fluorescent cell barcoding in flow cytometry-based immunophenotyping of leukocytes is applied. A novel approach of attachment combining two fluorescent dyes on the copolymer precursor and its conjugation to antibody is employed to synthesize barcoded nanoprobes of antibody polymer dyes allowing up to six nanoprobes to be resolved in two-dimensional cytometry analysis. The major advantage of these nanoprobes is the construct design in which the selected antibody is labeled with an advanced copolymer bearing two types of fluorophores in different molar ratios. The cells after antibody recognition and binding to the target antigen have a characteristic double fluorescence signal for each nanoprobe providing a unique position on the dot plot, thus allowing antibody-based barcoding of cellular samples in flow cytometry assays. This technique is valuable for cellular assays that require low intersample variability and is demonstrated by the live cell barcoding of clinical samples with B cell abnormalities. In total, the samples from six various donors were successfully barcoded using only two detection channels. This barcoding of clinical samples enables sample preparation and measurement in a single tube.
在此,应用了一种先进的生物偶联技术来合成针对荧光细胞条码的杂交聚合物-抗体纳米探针,该技术可用于基于流式细胞术的白细胞免疫表型分析。采用了一种将两种荧光染料结合在共聚物前体上并将其与抗体偶联的新方法,以合成带有抗体聚合物染料的条码纳米探针,从而可以在二维细胞术分析中分辨多达六个纳米探针。这些纳米探针的主要优势在于其结构设计,其中选择的抗体用带有两种不同摩尔比荧光团的先进共聚物进行标记。经过抗体识别和与靶抗原结合后,细胞对每个纳米探针具有特征性的双荧光信号,在点图上提供独特的位置,从而允许在流式细胞术检测中对细胞样本进行基于抗体的条码标记。该技术对于需要低样本间变异性的细胞分析非常有价值,并且通过对具有 B 细胞异常的临床样本进行活细胞条码标记得到了验证。总共,仅使用两个检测通道就成功地对来自六个不同供体的样本进行了条码标记。这种对临床样本的条码标记可以在单个管中进行样本制备和测量。