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High pressure freezing and freeze substitution reveal new aspects of fine structure and maintain protein antigenicity in barley aleurone cells
Author(s) -
Lonsdale Jennifer E.,
McDonald Kent L.,
Jones Russell L.
Publication year - 1999
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1046/j.1365-313x.1999.00362.x
Subject(s) - biology , aleurone , protoplast , hordeum vulgare , organelle , vacuole , antigenicity , biochemistry , microbiology and biotechnology , cytosol , cytoplasm , biophysics , enzyme , botany , antibody , poaceae , immunology
Summary High pressure freezing and freeze substitution (HPF‐FS) were used to prepare barley (Hordeum vulgareL. cv Himalaya) aleurone protoplasts for transmission electron microscopy (TEM). We show that HPF‐FS is superior to conventional chemical fixation and dehydration techniques for the preservation of cellular fine structure and antigenicity of proteins in barley aleurone protoplasts. HPF‐FS extracted fewer proteins from the cytosol and organelles of aleurone protoplasts and maintained the details of cellular structure. The cortical cytoskeleton, made up of microtubules, was observed for the first time by TEM in barley aleurone protoplasts prepared by HPF‐FS. Organelles such as protein storage vacuoles retained their proteinaceous contents, and other cellular organelles (including the Golgi apparatus, the nucleus and mitochondria) were also well preserved in protoplasts fixed by HPF‐FS. Antibodies to the vacuolar enzyme nuclease I, the tonoplast aquaporin α‐TIP and the glyoxysomal enzyme malate synthase showed that the antigenicity of organellar enzymes and membrane proteins was preserved in cells prepared by HPF‐FS. We conclude that HPF‐FS is superior to chemical fixation for the preparation of plant protoplasts for TEM and is the method of choice for the preservation of aleurone protoplasts for structural and immunochemical studies.