X-ray tomography of cryopreserved human prostate cancer cells: mitochondrial targeting by an organoiridium photosensitiser

Author:

Bolitho Elizabeth M.ORCID,Sanchez-Cano CarlosORCID,Huang HuaiyiORCID,Hands-Portman IanORCID,Spink MatthewORCID,Quinn Paul D.ORCID,Harkiolaki MariaORCID,Sadler Peter J.ORCID

Abstract

Abstract The organoiridium complex Ir[(C,N)2(O,O)] (1) where C, N = 1-phenylisoquinoline and O,O = 2,2,6,6-tetramethyl-3,5-heptanedionate is a promising photosensitiser for Photo-Dynamic Therapy (PDT). 1 is not toxic to cells in the dark. However, irradiation of the compound with one-photon blue or two-photon red light generates high levels of singlet oxygen (1O2) (in Zhang et al. Angew Chem Int Ed Engl 56 (47):14898-14902 10.1002/anie.201709082,2017), both within cell monolayers and in tumour models. Moreover, photo-excited 1 oxidises key proteins, causing metabolic alterations in cancer cells with potent antiproliferative activity. Here, the tomograms obtained by cryo-Soft X-ray Tomography (cryo-SXT) of human PC3 prostate cancer cells treated with 1, irradiated with blue light, and cryopreserved to maintain them in their native state, reveal that irradiation causes extensive and specific alterations to mitochondria, but not other cellular components. Such new insights into the effect of 1O2 generation during PDT using iridium photosensitisers on cells contribute to a detailed understanding of their cellular mode of action. Graphic abstract

Funder

Maria de Maeztu Units of Excellence Program from the Spanish State Research Agency

Diamond Light Source

Cancer Research UK

Gipuzkoa Foru Aldundia

Wellcome Trust

Engineering and Physical Sciences Research Council

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Biochemistry

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