Structured illumination microscopy using a photonic chip

被引:110
作者
Helle, Oystein Ivar [1 ]
Dullo, Firehun Tsige [1 ]
Lahrberg, Marcel [1 ]
Tinguely, Jean-Claude [1 ]
Helleso, Olav Gaute [1 ]
Ahluwalia, Balpreet Singh [1 ]
机构
[1] UiT Arctic Univ Norway, Dept Phys & Technol, Tromso, Norway
基金
欧洲研究理事会;
关键词
OPTICAL RECONSTRUCTION MICROSCOPY; FLUORESCENCE MICROSCOPY; RESOLUTION LIMIT; NANOSCOPY; REVEALS; COMPACT; PHASE;
D O I
10.1038/s41566-020-0620-2
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Structured illumination microscopy (SIM) enables live-cell super-resolution imaging of subcellular structures at high speeds. At present, linear SIM uses free-space optics to illuminate the sample with the desired light patterns; however, such arrangements are prone to misalignment and add cost and complexity to the microscope. Here, we present an alternative photonic chip-based two-dimensional SIM approach (cSIM) in which the conventional glass sample slide in a microscope is replaced by a planar photonic chip that importantly both holds and illuminates the specimen. The photonic chip reduces the footprint of the light illumination path of SIM to around 4 x 4 cm(2). An array of optical waveguides on the chip creates standing wave interference patterns at different angles, which illuminate the sample via evanescent fields. High-refractive-index silicon nitride waveguides allow a 2.3 times enhancement in imaging spatial resolution, exceeding the usual 2 times limit of SIM. In summary, cSIM offers a simple, stable and affordable approach for performing two-dimensional super-resolution imaging over a large field of view. The use of a photonic integrated circuit to both hold a biological sample and generate the necessary light patterns for structured illumination microscopy promises convenient super-resolution imaging.
引用
收藏
页码:431 / +
页数:11
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