Abstract

Many animals exhibit remarkable colors produced by the constructive interference of light reflected from arrays of intracellular guanine crystals. These systems are utilized for various purposes, including vision, camouflage, communication, and thermal regulation. Each guanine crystal forms within a membrane-bound organelle called an iridosome, where precise control over crystal formation occurs. While the presence of guanine crystals in iridosomes is well-documented, the mechanisms facilitating the accumulation of water-insoluble guanine and driving its crystallization remain unclear. Here, we employ advanced imaging and spectroscopy techniques to characterize the maturation of iridosomes in zebrafish iridophores during development. Using cryo-electron microscopy, we found that amorphous guanine accumulates in early-stage iridosomes. Synchrotron-based soft X-ray microscopy studies revealed that, unlike mature crystals, the accumulated guanine is initially in its protonated state. Live imaging with a pH sensor demonstrated that early-stage iridosomes are acidic and that their pH gradually approaches neutrality during maturation. Additionally, the application of a V-ATPase inhibitor reduced the acidity of iridosomes and significantly decreased crystal formation, suggesting the involvement of V-ATPase in regulating the organelle pH. Our findings reveal new insights into the molecular mechanisms facilitating guanine accumulation and crystallization within iridosomes, emphasizing the pivotal role of pH alternations in the precise formation of biogenic crystals.Competing Interest StatementThe authors have declared no competing interest.
Original languageEnglish
Article number2024.07.20.604036
JournalBioRxiv
DOIs
Publication statusIn preparation - 23 Jul 2024

Funding

This work was supported by an ERC Starting Grant (Grant number: 101077470, “CRYSTALCELL”) and by the Israel Science Foundation (grant No. 691/22) awarded to D.G. This work benefited from access to ALBA and has been supported by iNEXT-Discovery, project number 871037, funded by the Horizon 2020 program of the European Commission. Cryo soft X-ray experiments were performed at the MISTRAL Beamline at ALBA Synchrotron with the collaboration of ALBA staff. We thank Dr. Eva Pereiro for her support and assistance in coordinating with the synchrotron. Additionally, we thank Dr. Tali Lerer-Goldshtein for her support in developing the project’s experimental approach. Electron microscopy studies were conducted at the Irving and Cherna Moskowitz Center for Nano and Bio-Nano Imaging at the Weizmann Institute of Science.

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