Centre for Myopia Research, School of Optometry, The Hong Kong Polytechnic University, Hung Hom, Hong Kong.
Centre for Eye and Vision Research (CEVR), 17W Hong Kong Science Park, Hung Hom, Hong Kong.
Sci Data. 2024 Oct 10;11(1):1115. doi: 10.1038/s41597-024-03958-x.
The retina plays a crucial role in processing and decoding visual information, both in normal development and during myopia progression. Recent advancements have introduced a library-independent approach for data-independent acquisition (DIA) analyses. This study demonstrates deep proteome identification and quantification in individual mice retinas during myopia development, with an average of 6,263 ± 86 unique protein groups. We anticipate that the use of a predicted retinal-specific spectral library combined with the robust quantification achieved within this dataset will contribute to a better understanding of the proteome complexity. Furthermore, a comprehensive mice retinal-specific spectral library was generated, encompassing a total identification of 9,401 protein groups, 70,041 peptides, 95,339 precursors, and 761,868 transitions acquired using SWATH-MS acquisition on a ZenoTOF 7600 mass spectrometer. This dataset surpasses the spectral library generated through high-pH reversed-phase fractionation by data-dependent acquisition (DDA). The data is available via ProteomeXchange with the identifier PXD046983. It will also serve as an indispensable reference for investigations in myopia research and other retinal or neurological diseases.
视网膜在处理和解码视觉信息方面起着至关重要的作用,无论是在正常发育过程中还是近视进展过程中。最近的进展引入了一种独立于文库的数据独立采集 (DIA) 分析方法。本研究在近视发展过程中对单个小鼠视网膜进行了深度蛋白质组鉴定和定量分析,平均有 6,263 ± 86 个独特的蛋白质组。我们预计,使用预测的视网膜特异性光谱库,并结合该数据集内实现的强大定量方法,将有助于更好地理解蛋白质组的复杂性。此外,还生成了一个全面的小鼠视网膜特异性光谱库,该库总共鉴定了 9,401 个蛋白质组、70,041 个肽段、95,339 个前体和 761,868 个采用 SWATH-MS 采集在 ZenoTOF 7600 质谱仪上获得的跃迁。该数据集超过了通过数据依赖采集 (DDA) 的高 pH 反相分级分离生成的光谱库。该数据集可通过 ProteomeXchange 以标识符 PXD046983 获取。它还将成为近视研究和其他视网膜或神经疾病研究不可或缺的参考。