Go Eden P, Hewawasam Geetha S, Ma Ben J, Liao Hua-Xin, Haynes Barton F, Desaire Heather
Department of Chemistry, University of Kansas, Lawrence, KS.
Int J Mass Spectrom. 2011 Aug;305(2-3):209-216. doi: 10.1016/j.ijms.2010.11.009.
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's 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.
本文所展示的工作描述了对一种部分去糖基化的HIV疫苗候选包膜蛋白(Env)的首次全面分析。Env,即JRFL gp140 ΔCF,具有27个潜在糖基化位点,作为生成更具免疫原性的HIV疫苗策略的一部分,用PNGase F对其进行了部分去糖基化,并且使用两种不同的糖苷酶Endo H和Endo F3,通过独特的工作流程对所得蛋白质的糖基化进行了表征。这种独特的分析方案覆盖了27个糖基化位点中的26个,数据表明用PNGase F进行的生化处理产生了一种高度异质性的糖蛋白产物,该产物在大多数糖基化位点都已部分去糖基化。本文所述的方案可用于表征其他天然或经生化去糖基化的蛋白质的糖基化位点占据情况。