Difference between revisions of "Optical trap"
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Revision as of 16:20, 26 March 2013
Introduction
Optical tweezers can exert and measure forces on micron-scale dielectric particles. This capability offers a unique and valuable tool for manipulating and measuring cell components at the single molecule level. For example, optical traps have been used extensively to investigate the mechanical properties of biological polymers and the force generation mechanisms of molecular motors. In many studies, optical tweezers apply force to functionalized microspheres, which act as convenient handles attached to molecules of interest.
To make quantitative force measurements, the instrument records the displacement of a trapped microsphere over time. For small displacements, the exerted force is very nearly proportional to displacement, so the trap can be modeled as a linear spring. Accurate force and position measurements depend on careful calibration of the position detector responsivity, G, and the trap stiffness α, also called the spring constant. The stiffness is a function of trapping laser power, bead size, bead composition, and optical properties of the sample.
This page has tips for setting up and aligning an optical trap. It discusses three methods for obtaining the spring constant and two methods for measuring α.
Instrument overview
A high-NA objective lens (L1) performs the dual functions of imaging the sample and focusing the trapping laser. L1 is a 1.25 NA, 100X, infinity corrected, oil immersion objective lens with a working distance of 0.65 mm. Its back aperture is 5mm in diameter.
L7 focuses an image of the LED illuminator in the backplane of the condenser lens L2 to provide collimated transillumination in the sample plane. L2 is a .25 NA, 10X, infinity corrected objective lens with a 7 mm working distance. Steering mirror M1 and tube lens L3 complete the imaging path. L3 is a 1" diameter, uncoated plano convex lens with a focal length of 200 mm. L3 forms an image of the sample plane on the detector of a CCD camera placed at a distance of 200 mm. (For best performance, the distance between L3 and the CCD imager must be accurate.)
The trapping laser beam emerges from a fiber coupler with a diameter of approximately ??mm. Lenses L4 and L5 (focal lengths ?? and ??, respectively) implement a Galilean telescope that expands the beam by a factor of 4. To minimize aberrations and reflections, L4 and L5 are IR-coated achromatic doublet lenses. Dichroic mirror D1 deflects the collimated trapping beam toward L1.
Calibration
To make quantitative force measurements, the optical trap records the displacement of a trapped particle over time. For small displacements, the exerted force is very nearly proportional to displacement. In this range, the trap can be modeled as a linear spring. Accurate force and position measurements depend on careful calibration of the position detector responsivity, GQPD, and the trap stiffness α. GQPD and α are functions of the adjustment of the instrument, trapping laser power, bead size, bead composition, and optical properties of the sample. The instrument has to be calibrated for each type of sample and any time an adjustment is made. (Calibration can be sensitive to the angle of the sample chamber, so it is a good idea to recalibrate every time the sample is changed.)
Finding α
Several methods for measuring trap stiffness have been developed. Because the methods rely on different underlying principles, they tend to be sensitive to different types of experimental errors. Using multiple calibration methods can provide an important check on results.
The three methods are summarized in the following table.
Method | Equation | QPD Responsivity | Stage Responsivity | Solvent Viscosity | Particle Diameter | Temperature | Technical Noise |
---|---|---|---|---|---|---|---|
$ R_{QPD} $ | $ R_{stage} $ | $ \eta $ | $ d $ | $ T $ | |||
Equipartition | $ \frac{K_B T}{\langle R_{qpd} V_{qpd} \rangle ^ 2} $ | inverse square | none | none | none | linear and indirect (viscosity change) | systematic decrease |
PSD | $ \left. {6 \pi^2 \eta d \, f_0} \right. $ | none | none | linear | linear | indirect (viscosity change) | small |
Stokes | $ \langle \frac{3 \pi \eta d \, R_{stage} \, ^{d V_{stage}} / _{dt}} {R_{qpd} V_{qpd}} \rangle $ | inverse | linear | linear | linear | indirect (viscosity change) | none |
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Caption
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--- say something about QPD ----
Remove the optics
Collimating and adjusting the fiber port
Initial laser alignment
Beam expander coarse adjustment
Condenser adjustment
Connecting the piezo stage
Fine adjusting the beam expander
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OTKB software
Starting the software
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Calibration
Measuring R by scanning a stuck bead
PSD method
Equipartition method
Stokes method
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