Multifunctional encoded particles for high-throughput biomolecule analysis

被引:626
作者
Pregibon, Daniel C.
Toner, Mehmet
Doyle, Patrick S.
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] Massachusetts Gen Hosp, BioMEMS Resource Ctr, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Ctr Engn Med, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Boston, MA 02114 USA
关键词
D O I
10.1126/science.1134929
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
High-throughput screening for genetic analysis, combinatorial chemistry, and clinical diagnostics benefits from multiplexing, which allows for the simultaneous assay of several analytes but necessitates an encoding scheme for molecular identification. Current approaches for multiplexed analysis involve complicated or expensive processes for encoding, functionalizing, or decoding active substrates ( particles or surfaces) and often yield a very limited number of analyte-specific codes. We present a method based on continuous-flow lithography that combines particle synthesis and encoding and probe incorporation into a single process to generate multifunctional particles bearing over a million unique codes. By using such particles, we demonstrate a multiplexed, single-fluorescence detection of DNA oligomers with encoded particle libraries that can be scanned rapidly in a flow-through microfluidic channel. Furthermore, we demonstrate with high specificity the same multiplexed detection using individual multiprobe particles.
引用
收藏
页码:1393 / 1396
页数:4
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