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• W2036742807 abstract "The use of proteins for in vitro studies or as therapeutic agents is frequently hampered by protein aggregation during expression, purification, storage, or transfer into requisite assay buffers. A large number of potential protein stabilizers are available, but determining which are appropriate can take days or weeks. We developed a solubility assay to determine the best cosolvent for a given protein that requires very little protein and only a few hours to complete. This technique separates native protein from soluble and insoluble aggregates by filtration and detects both forms of protein by SDS-PAGE or Western blotting. Multiple buffers can be simultaneously screened to determine conditions that enhance protein solubility. The behavior of a single protein in mixtures and crude lysates can be analyzed with this technique, allowing testing prior to and throughout protein purification. Aggregated proteins can also be assayed for conditions that will stabilize native protein, which can then be used to improve subsequent purifications. This solubility assay was tested using both prokaryotic and eukaryotic proteins that range in size from 17 to 150 kDa and include monomeric and multimeric proteins. From the results presented, this technique can be applied to a variety of proteins." @default.
• W2036742807 created "2016-06-24" @default.
• W2036742807 creator A5037753501 @default.
• W2036742807 creator A5069025755 @default.
• W2036742807 date "2003-05-01" @default.
• W2036742807 modified "2023-10-17" @default.
• W2036742807 title "Detection and prevention of protein aggregation before, during, and after purification" @default.
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• W2036742807 doi "https://doi.org/10.1016/s0003-2697(03)00059-9" @default.
• W2036742807 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12711344" @default.
• W2036742807 hasPublicationYear "2003" @default.
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