The 2018 Nobel Prize in Physics: optical tweezers and chirped pulse amplification

Matthew C. Asplund, Jeremy A. Johnson, James E. Patterson

The 2018 Nobel Prize in Physics was awarded to Arthur Ashkin (prize share ½), Gérard Mourou (prize share ¼), and Donna Strickland (prize share ¼) for “groundbreaking inventions in the field of laser physics.” This feature article summarizes the development of “optical tweezers and their application to biological systems” by Arthur Ashkin, as well as the Mourou/Strickland method of “generating high-intensity, ultrashort optical pulses” known as chirped pulse amplification. Further developments are also briefly discussed.

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Optical tweezers for medical diagnostics

Christopher N. LaFratta
Laser trapping by optical tweezers makes possible the spectroscopic analysis of single cells. Use of optical tweezers in conjunction with Raman spectroscopy has allowed cells to be identified as either healthy or cancerous. This combined technique is known as laser tweezers Raman spectroscopy (LTRS), or Raman tweezers. The Raman spectra of cells are complex, since the technique probes nucleic acids, proteins, and lipids; but statistical analysis of these spectra makes possible differentiation of different classes of cells. In this article the recent development of LTRS is described along with two illustrative examples for potential application in cancer diagnostics. Techniques to expand the uses of LTRS and to improve the speed of LTRS are also suggested.
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Cell separation by the combination of microfluidics and optical trapping force on a microchip

Masaya Murata, Yukihiro Okamoto, Yeon-Su Park, Noritada Kaji, Manabu Tokeshi, and Yoshinobu Baba

We investigated properties of cells affecting their optical trapping force and successfully established a novel cell separation method based on the combined use of optical trapping force and microfluidics on a microchip. Our investigations reveal that the morphology, size, light absorption, and refractive index of cells are important factors affecting their optical trapping force. A sheath flow of sample solutions created in a microchip made sample cells flow in a narrow linear stream and an optical trap created by a highly focused laser beam captured only target cells and altered their trajectory, resulting in high-efficiency cell separation. An optimum balance between optical trapping force and sample flow rate was essential to achieve high cell separation efficiency. Our investigations clearly indicate that the on-chip optical trapping method allows high-efficiency cell separation without cumbersome and time-consuming cell pretreatments. In addition, our on-chip optical trapping method requires small amounts of sample and may permit high-throughput cell separation and integration of other functions on microchips.

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