Biochemical Analyses of Proteins from Duttaphrynus melanostictus (Bufo melanostictus) Skin Secretion: Soluble Protein Retrieval from a Viscous Matrix by Ion-Exchange Batch Sample Preparation
| Autor: | Marcela Di Giacomo Messias, Daniel C. Pimenta, Douglas Oscar Ceolin Mariano, Patrick Jack Spencer, José Pedro Prezotto-Neto |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Chromatography Molecular mass Hydrolases Chemistry Organic Chemistry Ion chromatography Extraction (chemistry) Analytical technique Bioengineering Fraction (chemistry) Chromatography Ion Exchange Biochemistry Amphibian Proteins Bufonidae Analytical Chemistry 03 medical and health sciences 030104 developmental biology Yield (chemistry) Animals Sample preparation Centrifugation Skin |
| Zdroj: | The Protein Journal. 37:380-389 |
| ISSN: | 1875-8355 1572-3887 |
| DOI: | 10.1007/s10930-018-9780-z |
| Popis: | A crucial step in scientific analysis can be sample preparation, and its importance increases in the same rate as the sensitivity of the following employed/desired analytical technique does. The need to analyze complex, viscous matrices is not new, and diverse approaches have been employed, with different success rates depending on the intended molecules. Solid-phase extraction, for example, has been successfully used in sample preparation for organic molecules and peptides. However, due to the usual methodological conditions, biologically active proteins are not successfully retrieved by this technique, resulting in a low rate of protein identification reported for the viscous amphibian skin secretion. Here we describe an ion-exchange batch processing sample preparation technique that allows viscous or adhesive materials (as some amphibian skin secretions) to be further processed by classical liquid chromatography approaches. According to our protocol, samples were allowed to equilibrate with a specific resin that was washed with appropriated buffers in order to yield the soluble protein fraction. In order to show the efficiency of our methodology, we have compared our results to classically prepared skin secretion, i.e., by means of filtration and centrifugation. After batch sample preparation, we were able to obtain reproductive resolved protein chromatographic profiles, as revealed by SDS-PAGE, and retrieve some biological activities, namely, hydrolases belonging to serine peptidase family. Not only that, but also the unbound fraction was rich in low molecular mass molecules, such as alkaloids and steroids, making this sample preparation technique also suitable for the enrichment of such molecules. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full text from SpringerLink