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    Fluorescence recovery after photobleaching (FRAP)

    Pietro De Camilli, Xinbo Wang

    Published: 2023-08-26 DOI: 10.17504/protocols.io.5qpvobj29l4o/v1
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    Abstract

    This protocol details methods of the FRAP analysis of LRRK2-induced liposome tubules in vitro

    Attachments

    iuufbvk9p.docx

    Steps

    Fluorescence recovery after photobleaching (FRAP)

    1.

    Prepare LRRK2-liposome mixtures in a PCR tube with 300nanomolar (nM) GFP-LRKK2, 20micromolar (µM) liposomes (labeled with trace amounts of rhodamine-PE) and 1millimolar (mM) GMPPNP.

    2.

    Immediately deposit6µL -10µL samples of step 1 on a 35 mm glass bottom dish and incubate at 37°C for 0h 30m 0s.

    Note
    Note: Drop some buffer in the dish to prevent samples from drying out due to evaporation during incubation.

    3.

    Perform FRAP experiments with a Spinning disk confocal (SDC) microscopy at Room temperature on a Nikon Ti-E inverted microscope using the Improvision UltraVIEW VoX system, with the settings as:

    3.1.

    Acquire the time-lapse images at every 0h 0m 15s.

    3.2.

    Acquire three images before bleaching.

    3.3.

    Bleach three ROIs with a 488 nm laser for 500 ms.

    3.4.

    Acquire post-bleach images up to 0h 10m 0s at 0h 0m 15s intervals.

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