Treffer: A barcode-specific immobilization interface for microfluidics-assisted uniform spatially barcoded microarray analysis.

Title:
A barcode-specific immobilization interface for microfluidics-assisted uniform spatially barcoded microarray analysis.
Authors:
Tian, Sidi1,2 (AUTHOR), Li, Yingxue2 (AUTHOR), Yao, Jia2 (AUTHOR), Huan, Changxiang1,2 (AUTHOR), Zhang, Wei2 (AUTHOR), Li, Shuli2 (AUTHOR), Zhang, Zhiqi2 (AUTHOR), Guo, Zhen2 (AUTHOR), Yang, Qi2 (AUTHOR), Li, Chao2 (AUTHOR), Li, Chuanyu2 (AUTHOR) lichy@sibet.ac.cn, Li, Jinze2 (AUTHOR) zhoulq@sibet.ac.cn, Zhou, Lianqun1,2 (AUTHOR)
Source:
Analyst. 10/21/2025, Vol. 150 Issue 20, p4586-4596. 11p.
Database:
Academic Search Index

Weitere Informationen

Microfluidics-assisted spatially barcoded microarray technology offers a high-throughput, low-cost approach towards spatial transcriptomic profiling. A uniform barcoded microarray is crucial for spatially unbiased mRNA analysis. However, non-specific adsorption of barcoding reagents in microchannels occurs during liquid transport, causing non-uniform barcoding in the chip's functional regions. The uneven microarray further leads to biased transcriptome capture. Herein, we develop a barcode-specific immobilization (BarSI) interface with both anti-adsorption properties and biological activity for the development of uniform spatially barcoded microarray chips. We immobilize DNA probes in straight and serpentine microchannels with coefficients of variation (CV) of 2.3% and 3.2%. Based on the orthogonal barcoding system, we developed spatially barcoded microarray chips with an overall fluorescence intensity CV of 8.47 ± 1.26%, compared with the CV of 20.91 ± 2.84% of microarrays developed on conventional amino glass slides. Using the uniform spatially barcoded microarray chip, we achieved spatially unbiased detection of mouse liver mRNA with an absolute value of Moran's I below 0.05. We present an economical and accessible method for manufacturing uniform spatially barcoded microarray chips, introducing a novel strategy for unbiased transcriptome analysis. [ABSTRACT FROM AUTHOR]