Localization of phytohemagglutinin in the embryonic axis of Phaseolus vulgaris with ultra-thin cryosections embedded in plastic after indirect immunolabeling
- 1 December 1984
- journal article
- research article
- Published by Springer Nature in Planta
- Vol. 162 (6) , 548-555
- https://doi.org/10.1007/bf00399921
Abstract
We have examined the properties and subcellular localization of phytohemagglutinin (PHA), the major lectin of the common bean (Phaseolus vulgaris.), in the axis cells of nearly mature and imbibed mature seeds. On a protein basis the axis contained about 15% as much PHA as the cotyledons. Localization of PHA was done with an indirect immunolabeling method (rabbit antibodies against PHA, followed by colloidal gold particles coated with goat antibodies against rabbit immunoglobulins) on ultra-thin cryosections which were embedded in plastic on the grids after the immunolabeling procedure. The embedding greatly improved the visualization of the subcellular structures. The small (4 nm) collodial gold particles, localized with the electron microscope, were found exclusively over small vacuoles or protein bodies in all the cell types examined (cortical parenchyma cells, vascular-bundle cells, epidermal cells). The matrix of these vacuoles-protein bodies appears considerably less dense than that of the protein bodies in the cotyledons, but the results confirm that in all parts of the embryo PHA is localized in similar structures.Keywords
This publication has 24 references indexed in Scilit:
- Biosynthesis, processing and transport of storage proteins and lectins in cotyledons of developing legume seedsPhilosophical Transactions of the Royal Society of London. B, Biological Sciences, 1984
- Immunocytochemical localization of wheat germ agglutinin in wheat.The Journal of cell biology, 1982
- “Western Blotting”: Electrophoretic transfer of proteins from sodium dodecyl sulfate-polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein AAnalytical Biochemistry, 1981
- Ultrastructural localization of soybean agglutinin on thin sections of Glycine max (soybean) var. Altona by the gold methodHistochemistry and Cell Biology, 1980
- Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proceedings of the National Academy of Sciences, 1979
- COMPARTMENTALIZATION IN THE COTYLEDONARY CELLS OF PHASEOLUS VULGARIS L. SEEDS: A DIFFERENTIAL SEDIMENTATION STUDYNew Phytologist, 1977
- Improved procedures for immunoferritin labeling of ultrathin frozen sections.The Journal of cell biology, 1976
- Purification and characterization of the major storage proteins of Phaseolus vulgaris seeds, and their intracellular and cotyledonary distributionPhytochemistry, 1976
- Purification of the phytohemagglutinin family of proteins from red kidney beans (Phaseolus vulgaris) by affinity chromatographyBiochimica et Biophysica Acta (BBA) - Protein Structure, 1975
- Development of Cotyledon Cell Structure in RipeningPhaseolus vulgarisSeedsJournal of Experimental Botany, 1968