Abstract

Capturing single cells from large heterogenous populations based solely on observable traits is necessary for many cell biology applications and remains a major technical challenge. The protocol we present allows the isolation of viable and metabolically active cells selected for their shape, migration speed, contact to other cells, or intracellular protein localization. We previously introduced a method termed Cell Labeling via Photobleaching (CLaP) for the efficient tagging of cells chosen for visual criteria. Here we describe a new protocol for capturing such cells using ferromagnetic beads termed single-cell magneto-optical capture (scMOCa). This technology is especially useful when the number of target cells represents an extremely low fraction of the total population (potentially one single cell), a situation in which conventional sorting techniques like fluorescent or magnetic activated cell sorting (F/MACS) cannot provide satisfactory results in terms of capture efficiency and specificity. scMOCa uses the lasers of a confocal microscope to photobleach and crosslink biotin-4-fluorecein molecules to cell membranes. Streptavidin coated magnetic beads then adhere to biotin moieties and a magnet allows the capture of illuminated cells. By precisely controlling liquid volumes and spacing between the different parts of a simple setup, high cell selectivity and capture efficacy can be achieved. scMOCA allows visual selection and isolation of any number of cells in a microscopy field and captured cells remain viable to generate new colonies of chosen phenotypes for downstream analyses.

Highlights

  • FACS or MACS cannot sort these cells since they are sensitive to the total signal intensity rather than its localization

  • Some situations involve cells for which there is a marker, but that are too rare to be efficiently extracted with FACS or MACS (Leary, 2000)

  • Rare mutated metastatic or transfected cells. scMOCA is optimized for low cell numbers and as such is an ideal technique in these situations

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Summary

Introduction

7. On the day the cells are plated, coat the chamber substrate with a solution of choice for improved cell adhesion (gelatin, poly-ornithine or collagen). 2. If the setup is built without Lego bricks, important parameters that must be kept constant are the distance between chambers (6 mm from the bottom of the donor chamber to the bottom of the collection chamber) and the ability to maintain 10 magnets close to a nail which head is centered in the collection chamber as shown Video 1.

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