量子点
纳米技术
材料科学
结合
物理
光电子学
数学
数学分析
作者
Vladimir L. Kolossov,Kaviamuthan Kanakaraju,Suresh Sarkar,Opeyemi H. Arogundade,Chia-Wei Kuo,Nathan A. Mara,Andrew M. Smith
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-05-30
卷期号:18 (23): 15084-15095
标识
DOI:10.1021/acsnano.4c02215
摘要
Antibodies and their conjugates of fluorescent labels are widely applied in life sciences research and clinical pathology. Among diverse label types, compact quantum dots (QDs) provide advantages of multispectral multiplexing, bright signals in the deep red and infrared, and low steric hindrance. However, QD-antibody conjugates have random orientation of the antigen-binding domain which may interfere with labeling and are large (20–30 nm) and heterogeneous, which limits penetration into biospecimens. Here, we develop conjugates of compact QDs and Fab′ antibody fragments as primary immunolabels. Fab′ fragments are conjugated site-specifically through sulfhydryl groups distal to antigen-binding domains, and the multivalent conjugates have small and homogeneous sizes (∼12 nm) near those of full-sized antibodies. Their performance as immunolabels for intracellular antigens is evaluated quantitatively by metrics of microtubule labeling density and connectivity in fixed cells and for cytological identification in fixed brain specimens, comparing results with probes based on spectrally-matched dyes. QD-Fab′ conjugates outperformed QD conjugates of full-sized antibodies and could be imaged with bright signals with 1-photon and 2-photon excitation. The results demonstrate a requirement for smaller bioaffinity agents and site-specific orientation for the success of nanomaterial-based labels to enhance penetration in biospecimens and minimize nonspecific staining.
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