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OS-SIM - Optical Sectioning Structured Illumination Microscopy

Learn how to build a low-cost, DMD-based Structured Illumination Microscope (SIM) for optical sectioning. This system removes out-of-focus blur and dramatically improves image contrast in fluorescence microscopy.

What is Optical Sectioning SIM?

Optical Sectioning SIM (OS-SIM) illuminates the sample with structured patterns (stripes) instead of uniform light. By acquiring multiple images with different pattern phases and combining them mathematically, you can extract in-focus information while suppressing out-of-focus background.

The RMS Reconstruction Algorithm

Three images are acquired with phase shifts (0°, 120°, 240°), then combined:

ISIM(x)=(I1I2)2+(I2I3)2+(I1I3)2I_{\text{SIM}}(x) = \sqrt{(I_1 - I_2)^2 + (I_2 - I_3)^2 + (I_1 - I_3)^2}

This computation removes out-of-focus blur, effectively creating optical sections without physically scanning.

Two Configurations

Direct Projection Setup

The DMD pattern is directly imaged onto the sample. Simple and easy to align, but includes all diffraction orders.

4f Interference Setup

Uses a Fourier filter to remove higher diffraction orders, creating cleaner interference patterns for improved optical sectioning.

What You'll Learn

  • Principles of structured illumination microscopy
  • DMD (Digital Micromirror Device) control
  • Optical sectioning without mechanical scanning
  • Pattern projection and phase shifting
  • Image reconstruction algorithms
  • 4f optical relay systems
  • Fourier filtering techniques

Tutorials in this Section

  • OS-SIM Tutorial - Complete guide to building a DMD-based SIM system

Key Components

Optical Components

  • 488nm laser (fiber-coupled)
  • 10× Plan Objective (NA = 0.25)
  • Tube lens (f = 100mm)
  • Projection lens (f = 200mm for direct setup)
  • Relay lenses (2× f = 50mm for 4f setup)
  • Dichroic mirror and emission filters
  • Spatial filter (for 4f configuration)

Electronics

  • DMD: DLP300S chip + DLPC1438 controller (from Anycubic Photon Ultra)
  • Controller: Raspberry Pi Zero 2
  • Interface: Custom bridge board (based on OpenMLA)
  • Power: 12V power supply

Mechanical

  • OpenUC2 cubes and mounting plates
  • Custom DMD mounting parts

How It Works

  1. Pattern Generation: DMD creates structured patterns (stripes)
  2. Projection: Pattern is imaged onto the sample
  3. Phase Shifting: Pattern shifts in 3 steps (0°, 120°, 240°)
  4. Image Acquisition: Camera captures one image per phase
  5. Reconstruction: Mathematical combination removes out-of-focus light

Safety Warning ⚠️

Laser Safety: This system uses a 488nm laser. Always wear appropriate safety goggles.

DMD Diffraction: The DMD acts as a grating, creating multiple diffraction orders. Ensure all stray beams are properly blocked to prevent eye exposure.

Key Advantages

  • No Mechanical Scanning: Purely electronic pattern switching
  • Low Cost: Uses harvested DMD from 3D printers
  • UC2 Integration: Works with existing UC2 fluorescence setups
  • True Optical Sectioning: Removes out-of-focus blur computationally
  • Fast Acquisition: Electronic pattern switching is rapid

Applications

  • Fluorescence microscopy with improved contrast
  • Thick sample imaging without confocal scanning
  • Live cell imaging with optical sectioning
  • Educational demonstrations of computational microscopy
  • Research into structured illumination techniques

Technical Capabilities

  • Optical sectioning without Z-scanning
  • Pattern frequency adjustable via DMD programming
  • Compatible with various fluorophores (488nm excitation)
  • Real-time or post-processing reconstruction
  • Integration with existing wide-field systems

Perfect for researchers and educators interested in advanced fluorescence microscopy techniques without the cost of commercial systems!