Analysis of glycosylphosphatidylinositol protein anchors: The prion protein

被引:27
作者
Baldwin, MA [1 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
来源
MASS SPECTROMETRY: MODIFIED PROTEINS AND GLYCOCONJUGATES | 2005年 / 405卷
关键词
D O I
10.1016/S0076-6879(05)05008-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Membrane proteins constitute a substantial fraction of the human proteome. A small subgroup associates with membranes through the presence of a C-terminal lipid anchor that is joined to the protein via a phosphoglycan. The prion protein (PrP), an abnormally folded form that causes fatal neurodegeneration, is one example of a glycosylphosphatidylinositol (GPI)-anchored protein. Although GPI-anchored proteins were first recognized some 20 years ago (in the mid-1980s), relatively few GPI anchors have been analyzed in detail. Therefore, a description of the analysis of the PrP-GPI anchor using a variety of mass spectrometric methods is of interest even though some of the approaches adopted could be facilitated through the use of newer, more sensitive techniques.
引用
收藏
页码:172 / 187
页数:16
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