4.6 Article

In-Depth Investigation of Low-Abundance Proteins in Matured and Filling Stages Seeds ofGlycine maxEmploying a Combination of Protamine Sulfate Precipitation and TMT-Based Quantitative Proteomic Analysis

Journal

CELLS
Volume 9, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/cells9061517

Keywords

soybean; basic pH reverse phase; filter-aided sample preparation; low-abundance proteins; maxquant; protamine sulfate precipitation; perseus; tandem mass tags

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Funding

  1. National Research Foundation of Korea (NRF) through the leading research supporting program [2019R1A2C2085868]
  2. Rural Development Administration (RDA) through Systems & Synthetic Agrobiotech Center (SSAC) [PJ013186032020]
  3. National Research Foundation of Korea (NRF) through the next generation supporting program [2019R1A6A3A13095655]
  4. Ramalingaswami re-entry fellowship from the Department of Biotechnology, Ministry of Science and Technology, Government of India [BT/HRD/35/02/2006]
  5. National Research Foundation of Korea [2019R1A6A3A13095655, 2019R1A2C2085868] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. Rural Development Administration (RDA), Republic of Korea [PJ013186032020] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Despite the significant technical advancements in mass spectrometry-based proteomics and bioinformatics resources, dynamic resolution of soybean seed proteome is still limited because of the high abundance of seed storage proteins (SSPs). These SSPs occupy a large proportion of the total seed protein and hinder the identification of low-abundance proteins. Here, we report a TMT-based quantitative proteome analysis of matured and filling stages seeds of high-protein (Saedanbaek) and low-protein (Daewon) soybean cultivars by application of a two-way pre-fractionation both at the levels of proteins (by PS) and peptides (by basic pH reverse phase chromatography). Interestingly, this approach led to the identification of more than 5900 proteins which is the highest number of proteins reported to date from soybean seeds. Comparative protein profiles of Saedanbaek and Daewon led to the identification of 2200 and 924 differential proteins in mature and filling stages seeds, respectively. Functional annotation of the differential proteins revealed enrichment of proteins related to major metabolism including amino acid, major carbohydrate, and lipid metabolism. In parallel, analysis of free amino acids and fatty acids in the filling stages showed higher contents of all the amino acids in the Saedanbaek while the fatty acids contents were found to be higher in the Daewon. Taken together, these results provide new insights into proteome changes during filling stages in soybean seeds. Moreover, results reported here also provide a framework for systemic and large-scale dissection of seed proteome for the seeds rich in SSPs by two-way pre-fractionation combined with TMT-based quantitative proteome analysis.

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