Single-frame 3D fluorescence microscopy with ultraminiature lensless FlatScope

被引:167
作者
Adams, Jesse K. [1 ,2 ,3 ]
Boominathan, Vivek [2 ,3 ]
Avants, Benjamin W. [2 ]
Vercosa, Daniel G. [1 ,2 ]
Ye, Fan [2 ,3 ]
Baraniuk, Richard G. [2 ,3 ]
Robinson, Jacob T. [1 ,2 ,3 ,4 ,5 ]
Veeraraghavan, Ashok [1 ,2 ,3 ]
机构
[1] Rice Univ, Appl Phys Program, 6100 Main St, Houston, TX 77005 USA
[2] Rice Univ, Dept Elect & Comp Engn, Houston, TX 77005 USA
[3] Rice Univ, Nanophoton Computat Imaging & Sensing Lab, Houston, TX 77005 USA
[4] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
[5] Baylor Coll Med, Dept Neurosci, One Baylor Plaza, Houston, TX 77030 USA
基金
美国国家科学基金会;
关键词
CHIP; FILTER;
D O I
10.1126/sciadv.1701548
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
Modern biology increasingly relies on fluorescence microscopy, which is driving demand for smaller, lighter, and cheaper microscopes. However, traditional microscope architectures suffer from a fundamental trade-off: As lenses becomesmaller, theymust either collect less light or image a smaller field of view. To break this fundamental trade-off between device size and performance, we present a new concept for three-dimensional (3D) fluorescence imaging that replaces lenses with an optimized amplitude mask placed a few hundred micrometers above the sensor and an efficient algorithm that can convert a single frame of captured sensor data into high-resolution 3D images. The result is FlatScope: perhaps the world's tiniest and lightest microscope. FlatScope is a lensless microscope that is scarcely larger than an image sensor (roughly 0.2 g in weight and less than 1mmthick) and yet able to produce micrometer-resolution, high-frame rate, 3D fluorescence movies covering a total volume of several cubic millimeters. The ability of FlatScope to reconstruct full 3Dimages froma single frame of captured sensor data allows us to image 3Dvolumes roughly 40,000 times faster than a laser scanning confocal microscope while providing comparable resolution. We envision that this new flat fluorescence microscopy paradigm will lead to implantable endoscopes that minimize tissue damage, arrays of imagers that cover large areas, and bendable, flexible microscopes that conform to complex topographies.
引用
收藏
页数:9
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