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    Proximity Ligation Assay (PLA)

    Leonardo A Parra-Rivas

    Published: 2023-11-12 DOI: 10.17504/protocols.io.j8nlko6ydv5r/v1
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    Abstract

    Proximity Ligation Assay (PLA)

    Steps

    1.

    The PLA assay was performed as described previously with minor modifications 48. The following antibodies were used for the PLA experiments: Syn 204 against h-αSyn (Santa Cruz Biotechnology Cat# sc-32280, RRID:AB_628319)(1:100) and EPR12790 against VAMP-2 (Abcam Cat#

    ab214590)(1:300).

    2.

    The in-situ PLA was performed on fixed primary neurons

    with DuoLink PLA technology probes and reagents (Sigma-Aldrich Cat# DUO92002,

    DUO92004, DUO82049, DUO92008, and DUO92014), following the manufacturer’s

    protocol. First, the neurons were permeabilized with PBS + 0.4% Triton X-100

    for 10 min.

    3.

    After two PBS washes, the cells were incubated with a blocking

    solution for 2 hours at 37 °C and then incubated with the primary antibodies

    for 30 min at room temperature.

    4.

    The coverslips were washed twice for 5 min with

    buffer A, followed by incubation with the PLA probes (secondary antibodies

    against two different species bound to two oligonucleotides: anti-mouse MINUS (Sigma-Aldrich Cat#

    DUO92004 (also DUO92004-30RXN, DUO92004-100RXN), RRID:AB_2713942) and anti-rabbit PLUS) (Bethyl Cat# OLK-92002-0100,

    RRID:AB_10950581)in antibody diluent for 30 min at 37 °C. After two washes of 5

    min with buffer A, the ligation step was performed with ligase diluted in

    ligation stock for 30 min at 37 °C.

    5.

    The coverslips were washed with buffer A

    twice for 2 min before incubation for 50 min with amplification stock solution

    at 37 °C. After two washes of 10 min with buffer B. Finally, the coverslips

    were washed with PBS and mounted with Duoli in situ tu mounting medium

    (Sigma-Aldrich Cat# DUO82040-5 ML).

    6.

    A negative control experiment was performed

    for every antibody, where only one antibody was incubated with the PLA probes.

    The experiments were performed 2 times. The experiments were performed 2 times.

    Average signal intensities were measured using the  MetaMorph Microscopy Automation and Image

    Analysis Software (RRID:SCR_00236 http://www.moleculardevices.com/products/cellular-imaging-systems/acquisition-and-analysis-software/metamorph-microscopy#gref) http://www.moleculardevices.com/products/cellular-imaging-systems/acquisition-and-analysis-software/metamorph-microscopy#grefgref) and plotted using GraphPad Prism

    software [(RRID:SCR_002798) http://www.graphpad.com/].

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