Bright-Field Microscopy Visualization of Proteins and Protein Complexes by In Situ Proximity Ligation with Peroxidase Detection
Authors: Agata Zieba(1), Carolina Wählby, Fredrik Hjelm(2), Lee Jordan(3), Jonathan Berg(3), Ulf Landegren(1), Katerina Pardali(1)
(1) Dept. of Genetics and Pathology, UU
(2) Olink Bioscience, Uppsala
(3) Ninewells Hospital and Medical School, University of Dundee, Scotland, UK
Journal: Clinical Chemistry, 56(1), pp. 99-110
Abstract: BACKGROUND: The in situ proximity ligation assay (PLA) allows a
protein or protein complex to be represented as an amplifiable DNA
molecule. Recognition is mediated by proximity probes consisting of
antibodies coupled with oligonucleotides. Upon dual binding of the
proximity probes, the oligonucleotides direct the formation of a
circular DNA molecule, which is then amplified by rolling-circle
replication. The localized concatemeric product is then detected with
fluorescent probes. The in situ PLA enables localized detection of
individual native proteins or interacting protein pairs in fixed cells
or tissue sections, thus providing an important tool for basic and
clinical research.
METHODS: We used horseradish peroxidase (HRP)conjugated
oligonucleotides to couple in situ PLA with enzymatic visualization of
the localized detection event.
RESULTS: We demonstrate the detection of protein complexes, both in
cells and in tissue sections, and show that we can quantify the
complexes with image-analysis software specially developed for
recognizing HRP signals in bright-field microscopy images. We show
that fluorescence and HRP signals produce equivalent results, both ill
cultured cells and in tissue samples.
CONCLUSIONS: The combination of in situ PLA with bright-field
detection and automated image analysis allows the signals present to
be Counted in an automated fashion and thus provides a sensitive and
specific method for quantification of proteins and protein complexes
with bright-field microscopy. With this approach, in situ PLA can be
used without the requirement for expensive fluorescence microscopes,
thereby avoiding problems with nonspecific fluorescence while
maintaining compatibility with conventional histologic staining.