DOI: 10.1021/acsomega.6c03325 ISSN: 2470-1343

A Basic Matrix Protein Songin Selectively Promotes Aragonite Aggregation and Modulates Calcium Carbonate Crystallization in Hyriopsis cumingii

Leyu Fan, Jiali Liu, Maoxiao Peng, Xiaojun Liu

Abstract

In China, the pearl industry of Hyriopsis cumingii contributes approximately 80% of pearl production. Matrix proteins play crucial roles in shell and pearl biomineralization. However, the functions of basic matrix proteins in H. cumingii remain poorly understood. In this study, we identified a novel predicted secreted basic matrix protein, designated Songin, from the freshwater pearl mussel H. cumingii. Functional assays were performed using a chemically synthesized 53-amino-acid peptide corresponding to the predicted mature region of Songin. Songin transcripts showed a relative mantle-enriched expression pattern and were detected in dorsal mantle epithelial cells, suggesting a potential association with shell biomineralization. In the end point crystallization assay, Songin was associated with pronounced aggregation of mineral particles under Mg2+-containing aragonite-favoring conditions while exerting only minor effects on particle morphology in the calcite-favoring system. Raman spectroscopy supported the predominant polymorph assignments in the calcite-favoring and Mg2+-containing aragonite-favoring systems, and no obvious Songin-associated change in the predominant polymorph was detected under the tested conditions. Laser scanning confocal microscopy showed heterogeneous Cy5-associated fluorescence near localized regions of some mineral particles. Because free Cy5 and Cy5-labeled BSA controls were not included, nonspecific dye adsorption cannot be excluded, and these observations are regarded as preliminary qualitative information rather than evidence of specific crystal-surface binding. This study indicates that the synthetic mature-region Songin peptide was associated with pronounced mineral-particle aggregation under Mg2+-containing aragonite-favoring conditions in vitro, suggesting a potential role in mineral-particle assembly during shell biomineralization. These findings provide preliminary insight into the possible involvement of Songin in shell biomineralization.

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