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Detecting Electrons: CCD vs Film

Comprehensive guide comparing CCD and film detectors for electron microscopy, covering basic concepts, Fourier transforms, detector-specific terms, and practical evaluation methods. Learn about Nyquist frequency, dynamic range, quantum efficiency, and more, with practical tips on data evaluation and normalization techniques.

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Detecting Electrons: CCD vs Film

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  1. Detecting Electrons: CCD vs Film Practical CryoEM Course July 26, 2005 Christopher Booth

  2. Overview • Basic Concepts • Detector Quality Concepts • How Do Detectors Work? • Practical Evaluation Of Data Quality • Final Practical Things To Remember

  3. Basic Concepts • Fourier Transform and Fourier Space • Convolution • Transfer Functions • Point Spread Function • Modulation Transfer Function • Low Pass Filter

  4. Fourier Transform The co-ordinate (ω) in Fourier space is often referred to as spatial frequency or just frequency

  5. Graphical Representation Of The Fourier Transform

  6. Convolution

  7. Convolution In Fourier Space • Convolution in Real Space is Multiplication in Fourier Space • It is a big advantage to think in Fourier Space

  8. Low Pass Filter • Reducing or removing the high frequency components • Only the low frequency components are able to “pass” the filter x =

  9. Transfer Functions • A transfer function is a representation of the relation between the input and output of a linear time-invariant system • Represented as a convolution between an input and a transfer function

  10. Transfer Functions • In Fourier Space this representation is simplified = x

  11. Point Spread Function (PSF) • The blurring of an imaginary point as it passes through an optical system • Convolution of the input function with a

  12. Modulation Transfer Function (MTF) • A representation of the point spread function in Fourier space = x

  13. Summarize Basic Concepts • Fourier Transform and Fourier Space • Convolution describes many real processes • Convolution is intuitive in Fourier Space • Transfer Functions are multiplication in Fourier Space • MTF is the Fourier Transform Of the PSF • MTF is a Transfer Function • Some Filters are easiest to think about in Fourier Space

  14. Detector Specific Concepts • Nyquist Frequency • Dynamic Range • Linearity • Dark Noise

  15. Nyquist Frequency • Nyquist-Shannon Sampling Theorem • You must sample at a minimum of 2 times the highest frequency of the image • This is very important when digitizing continuous functions such as images

  16. Example Of Sampling Below Nyquist Frequency

  17. Quantum Efficiency • The Quantum Efficiency of a detector is the ratio of the number of photons detected to the number of photons incident

  18. Dynamic Range • The ratio between the smallest and largest possible detectable values. • Very important for imaging diffraction patterns to detect weak spots and very intense spots in the same image

  19. Linearity • Linearity is a measure of how consistently the CCD responds to light over its well depth. • For example, if a 1-second exposure to a stable light source produces 1000 electrons of charge, 10 seconds should produce 10,000 electrons of charge

  20. Summarize CCD Specific Terms • Nyquist Frequency, must sample image at 2x the highest frequency you want to recover

  21. So Why Does Anyone Use Film? • For High Voltage Electron Microscopes, the MTF of Film is in general better than that of CCD at high spatial frequencies. • If you have an MTF that acts like a low pass filter, you may not be able to recover the high resolution information

  22. How a CCD Detects electrons

  23. Electron Path After Striking The Scintillator 100 kV 200 kV 300 kV 400 kV

  24. How Readout Of the CCD Occurs

  25. How Film Detects Electrons Incident electrons Silver Emulsion Film

  26. Silver Grain Emulsion At Various Magnification

  27. How Film Is Scanned Incident Light Developed Silver Emulsion Film Scanner CCD Array

  28. Options For Digitizing Film

  29. Summary Of Detection Methods • Scintillator and fiber optics introduce some degredation in high resolution signal in CCD cameras • Film + scanner optics introduce a negligible amount of degredation of high resolution signal

  30. Practical Evaluation Of The CCD Camera

  31. Decomposing Graphite Signal x x

  32. Calculating Spectral Signal To Noise Ratio • Signal To Noise Ratio is more meaningful if we think in Fourier Space

  33. Calculating The Fourier Transform Of an Image • Image Of Carbon Film • amorphous (non crystalline) specimen • not beam sensitive • common Also called the power spectrum of the image

  34. Power Spectrum Of Amorphous Carbon On Film and CCD

  35. Comparing The Signal To Noise Ratio From Film and CCD

  36. Film Vs CCD Head-To-Head

  37. Calculating SNR for Ice Embedded Cytoplasmic Polyhedrosis Virus

  38. Reconstruction To 9 Å Resolution

  39. Confirming A 9 Å Structure

  40. Relating SNR(s) To Resolution 2/5 Nyquist Frequency

  41. Further Experimental Confirmation Of 2/5 Nyquist Table 2: Comparison of Reconstruction Statistics between Several Different Ice Embedded Single Particles Collected On the Gatan 4kx4k CCD at 200 kV at the Indicated Nominal Magnification

  42. Evaluate Your Data To Estimate The Quality Of Your Imaging • You can use ctfit from EMAN to calculate a spectral signal to noise ratio • Built In Method • Alternate Method Presented Here

  43. Final Practical Things to Remember… • Good Normalization Means Good Data • Dark Reference • Gain Normalization • Quadrant Normalization • Magnification Of CCD relative to Film • Angstroms/Pixel

  44. Normalization • Standard Normalization • Quadrant Normalization

  45. Quadrant Normalization

  46. Dark Reference

  47. Gain Normalization

  48. How Do I Tell If Something Is Wrong?

  49. Magnification Of CCD relative to Film • 2010F Mag x 1.38 = 2010F CCD Mag • 3000SFF Mag x 1.41 = 3000SFF CCD Mag • This has to be calibrated for each microscope detector.

  50. How Do I Calculate Angstroms/Pixel? • Å/pixel = Detector Step-Size/Magnification • For a microscope magnification of 60,000 on the 3000SFF: • Å /pixel = 150,000 Å / (microscope magnification x 1.41) • Å /pixel = 150,000 Å / (60,000 x 1.41)Å /pixel = 1.77

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