Repurposing a photosynthetic antenna protein as a super-resolution microscopy label. Issue 1 (December 2017)

• Record Type: Journal Article
• Authors: Barnett, Samuel; Hitchcock, Andrew; Mandal, Amit; Vasilev, Cvetelin; Yuen, Jonathan; Morby, James; Brindley, Amanda; Niedzwiedzki, Dariusz; Bryant, Donald; Cadby, Ashley; Holten, Dewey; Hunter, C.
• Is Part Of: Scientific reports. Volume 7:Issue 1(2017)
• Page Start: 1
• Page End: 11
• Publication Date: 2017-12
• Subjects: Natural history -- Research -- Periodicals; Biology -- Research -- Periodicals; Physical sciences -- Research -- Periodicals; Earth sciences -- Research -- Periodicals; Environmental sciences -- Research -- Periodicals; 502.85
• DOI: 10.1038/s41598-017-16834-z
• Languages: English
• ISSNs: 2045-2322

Abstract

Abstract Techniques such as Stochastic Optical Reconstruction Microscopy (STORM) and Structured Illumination Microscopy (SIM) have increased the achievable resolution of optical imaging, but few fluorescent proteins are suitable for super-resolution microscopy, particularly in the far-red and near-infrared emission range. Here we demonstrate the applicability of CpcA, a subunit of the photosynthetic antenna complex in cyanobacteria, for STORM and SIM imaging. The periodicity and width of fabricated nanoarrays of CpcA, with a covalently attached phycoerythrobilin (PEB) or phycocyanobilin (PCB) chromophore, matched the lines in reconstructed STORM images. SIM and STORM reconstructions ofEscherichia coli cells harbouring CpcA-labelled cytochromebd 1 ubiquinol oxidase in the cytoplasmic membrane show that CpcA-PEB and CpcA-PCB are suitable for super-resolution imagingin vivo . The stability, ease of production, small size and brightness of CpcA-PEB and CpcA-PCB demonstrate the potential of this largely unexplored protein family as novel probes for super-resolution microscopy.