The biological role of GPI anchors is of paramount importance; however, we are still far from fully understanding the structure–function relationship of these molecules. One major limiting factor has been the tiny quantities available from natural sources; obtaining homogeneous and well-defined GPI structures by synthesis, is both a challenge and an attractive goal. We report here the convergent synthesis of the essential core of the human GPI anchor 1, exploiting a common precursor to obtain the trisaccharidic donor 2 and a novel protecting groups sequence. The final product, prepared for the first time, is biologically active.
Synthesis of the essential core of the human glycosylphosphatidylinositol (GPI) anchor / B. Richichi; L. Luzzatto; R. Notaro; G. la Marca; C. Nativi. - In: BIOORGANIC CHEMISTRY. - ISSN 0045-2068. - STAMPA. - 39:(2011), pp. 88-93. [10.1016/j.bioorg.2010.12.002]
Synthesis of the essential core of the human glycosylphosphatidylinositol (GPI) anchor
RICHICHI, BARBARA;LA MARCA, GIANCARLO;NATIVI, CRISTINA
2011
Abstract
The biological role of GPI anchors is of paramount importance; however, we are still far from fully understanding the structure–function relationship of these molecules. One major limiting factor has been the tiny quantities available from natural sources; obtaining homogeneous and well-defined GPI structures by synthesis, is both a challenge and an attractive goal. We report here the convergent synthesis of the essential core of the human GPI anchor 1, exploiting a common precursor to obtain the trisaccharidic donor 2 and a novel protecting groups sequence. The final product, prepared for the first time, is biologically active.File | Dimensione | Formato | |
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