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Spatial Proteomics

MACSima image

Spatial proteomics is a term describing a wide variety of methods used to generate highly multiplexed images of specimens to characterise their protein composition and spatial organisation.  Unlike traditional proteomics which average results and lose spatial context, spatial proteomics reveals protein distributions (and hence cell properties) across intact tissue slices, enabling a detailed understanding of protein/cell networks, spatial relationships, and how local microenvironments influence and change with biological processes and disease.

The Imaging Facility's spatial proteomics platform is a Miltenyi MACSima. Using cyclic immunofluorescence (cycIF), this system can theoretically image an unlimited number of targets in one sample with the sequential addition, imaging and removal of labelled antibodies. The system is fully automated, uses samples prepared on standard microscope slides and does not require the use of proprietary antibodies.

Our system:

Miltenyi MACSima

Fully automated spatial proteomics cyclic immunofluorescence imaging platform

Wide-field epifluorescence microscope

Four channel detection (blue, green, red, far-red)

2x, 20x/0.75, 20x/0.45 objectives

Two techniques signal removal: photobleaching of primary conjugated antibodies or antibody release by enzymatic reaction

Automate liquid handling system

Ultraprecise stage for loading sample carriers

Hardware and image-based autofocus

MACS iQ view analysis software for imaging processing (multiplex fluorescence visualisation, segmentation, interactive gating, data analyses, multiple plotting options, workflow editor, distance analyses)

MACSima system