A highly sens,tive fluorescent staining method for detecting glycosylated proteins on SDS-polyacrylamide gel has been described. The carbohydrate groups in glycoproteins were oxidized with periodate on SDS-polyacrylamide gel to generate aldehyde groups which were subsequently labeled with a fluoresc
Improved Method for Detecting Fluorescent-Labeled Glycoprotein on Sodium Dodecyl Sulfate–Polyacrylamide Gel
✍ Scribed by Xiang Gao; Wang-Yi Liu; Kangcheng Ruan
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 167 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0045-2068
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✦ Synopsis
An improved method for detecting glycoproteins labeled with fluorescent probe on SDS-polyacrylamide gel has been developed based on the previous method we reported previously. In the current method, instead of dansyl glycyl hydrazide (DNS-GLY-NHNH 2 ), fluorescein 5-thiosemicarbazide with a high extinction coefficient and fluorescence quantum yield was employed to label glycoprotein covalently, and the fluorescent staining of glycoproteins on the gel after SDS-PAGE used in the previous method was replaced by the fluorescent labeling of protein samples before electrophoresis to save the fluorescent probe and to shorten the experiment period. Labeled glycoproteins can be detected clearly under ultraviolet illumination after electrophoresis. The examination of several known glycoproteins indicated that the limiting detective sensitivity in the current method was about 1-2 ng of glycoproteins tested, 10-20 times higher than that in the previous method.
📜 SIMILAR VOLUMES
A method for detection of glycoproteins in thin sodium dodecyl sulfate polyacrylamide gels was developed by a combination of (i) initial periodic acid oxidation/Alcian blue staining and (ii) subsequent staining with silver nitrate. The procedure allowed detection of as little as \(1.6 \mathrm{ng}\)
dling and storage. The overall quality ofthe second-dimension gel is improved by eliminating the dark carrier ampholyte streak at the front of the basic end of the gel as well as the SDS-Triton artifact at the acidic end. The degree of protein resolution is essentially identical for the two techniqu