Label‐Free Nanoimaging of Neuromelanin in the Brain by Soft X‐ray Spectromicroscopy. Issue 29 (14th May 2020)

• Record Type: Journal Article
• Authors: Brooks, Jake; Everett, James; Lermyte, Frederik; Tjhin, Vindy Tjendana; Banerjee, Samya; O'Connor, Peter B.; Morris, Christopher M.; Sadler, Peter J.; Telling, Neil D.; Collingwood, Joanna F.
• Is Part Of: Angewandte Chemie international edition. Volume 59:Issue 29(2020)
• Page Start: 11984
• Page End: 11991
• Publication Date: 2020-05-14
• Subjects: iron -- neuromelanin -- Parkinson's disease -- synchrotron imaging -- x-ray absorption spectroscopy; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.202000239
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: A hallmark of Parkinson's disease is the death of neuromelanin‐pigmented neurons, but the role of neuromelanin is unclear. The in situ characterization of neuromelanin remains dependent on detectable pigmentation, rather than direct quantification of neuromelanin. We show that direct, label‐free nanoscale visualization of neuromelanin and associated metal ions in human brain tissue can be achieved using synchrotron scanning transmission x‐ray microscopy (STXM), through a characteristic feature in the neuromelanin x‐ray absorption spectrum at 287.4 eV that is also present in iron‐free and iron‐laden synthetic neuromelanin. This is confirmed in consecutive brain sections by correlating STXM neuromelanin imaging with silver nitrate‐stained neuromelanin. Analysis suggests that the 1s–σ* (C−S) transition in benzothiazine groups accounts for this feature. This method illustrates the wider potential of STXM as a label‐free spectromicroscopy technique applicable to both organic and inorganic materials. Abstract : Soft X‐ray spectromicroscopy enables neuromelanin visualization in human brain tissue. This removes dependence on optical evaluation of pigmentation or chemical staining, opening the door to investigating relationships between depigmentation, metal binding, and neurodegeneration in the most vulnerable neurons in Parkinson's disease. (Image of brain adapted, under license CCBY4.0, from Blausen.com staff, WikiJournal of Medicine 2014, 1, ISSN 2002–4436.)