کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1192302 | 1492307 | 2011 | 8 صفحه PDF | دانلود رایگان |

The work presented herein describes the first comprehensive analysis of a partially deglycosylated HIV vaccine candidate envelope protein (Env). The Env, JRFL gp140 ΔCF, with 27 potential glycosylation sites, was partially deglycosylated with PNGase F as part of a strategy to generate a more immunogenic HIV vaccine, and the resulting protein glycosylation was characterized in a unique workflow using two different glycosidases, Endo H and Endo F3. This unique analysis protocol provided for coverage on 26 of the 27 glycosylation sites, and the data showed that the biochemical treatment with PNGase F resulted in a highly heterogeneous glycoprotein product that had been partially deglycosylated at most of the glycosylation sites. The protocols described in this work could be useful for characterizing the glycosylation site occupancy of other native or biochemically deglycosylated proteins.
Figure optionsDownload high-quality image (153 K)Download as PowerPoint slideResearch highlights▶ A new method for profiling glycosylation site occupancy is introduced. ▶ The method was applied to a partially deglycosylated Env glycoprotein, which is an HIV vaccine candidate. ▶ Partial deglycosylation of Env glycoproteins produces a highly heterogeneous product.
Journal: International Journal of Mass Spectrometry - Volume 305, Issues 2–3, 15 August 2011, Pages 209–216