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Brain ankyrin. Purification of a 72,000 Mr spectrin-binding domain
Abstract:
Polypeptides of Mr = 190,000-220,000 that cross-react with erythrocyte ankyrin were detected in immunoblots of membranes from pig lens, pig brain, and rat liver. The cross-reacting polypeptides from brain were cleaved by chymotrypsin to fragments of Mr = 95,000 and 72,000 which are the same size as fragments obtained with erythrocyte ankyrin. The brain 72,000 Mr fragment associated with erythrocyte spectrin, and the binding occurred at the same site as that of erythrocyte ankyrin 72,000 Mr fragment since (a) brain 72,000 Mr fragment was adsorbed to erythrocyte spectrin-agarose and (b) 125I-labeled erythrocyte spectrin bound to brain 72,000 Mr fragment following transfer of the fragment from a sodium dodecyl sulfate gel to nitrocellulose paper, and this binding was displaced by erythrocyte ankyrin 72,000 Mr fragment. Brain 72,000 Mr fragment was purified about 400-fold by selective extraction and by continuous chromatography on columns attached in series containing DEAE-cellulose followed by erythrocyte spectrin coupled to agarose, and finally hydroxylapatite. The brain 72,000 Mr fragment was not derived from contaminating erythrocytes since peptide maps of pig brain and pig erythrocyte 72,000 Mr fragments were distinct. The amount of brain 72,000 Mr fragment was estimated as 0.28% of membrane protein or 39 pmol/mg based on radioimmunoassay with 125I-labeled brain fragment and antibody against erythrocyte ankyrin. Brain spectrin tetramer was present in about the same number of copies (30 pmol/mg of membrane protein) based on densitometry of Coomassie blue-stained sodium dodecyl sulfate gels. The binding site on brain spectrin for both brain and erythrocyte ankyrin 72,000 Mr fragments was localized by electron microscopy to the midregion of spectrin tetramers about 90 nM from the near end and 110 nM from the far end. These studies demonstrate the presence in brain membranes of a protein closely related to erythrocyte ankyrin, and are consistent with a function of the brain ankyrin as a membrane attachment site for brain spectrin.
Insights
Researchers found a protein in pig brain membranes similar to erythrocyte ankyrin. This brain ankyrin binds to brain spectrin, suggesting a role in membrane structure.
Area of Science:
- Biochemistry
- Cell Biology
- Neuroscience
Background:
- Ankyrin is a key protein in red blood cell membranes, linking spectrin to the lipid bilayer.
- The presence and function of ankyrin in non-erythroid cells, such as brain, are less understood.
Purpose of the Study:
- To investigate the presence and characteristics of ankyrin-like proteins in pig brain membranes.
- To determine if brain ankyrin interacts with brain spectrin and to characterize this interaction.
Main Methods:
- Immunoblotting using antibodies against erythrocyte ankyrin.
- Chymotrypsin cleavage and fragment analysis.
- Binding assays with erythrocyte spectrin-agarose and 125I-labeled spectrin.
- Purification of brain ankyrin fragment via chromatography.
- Peptide mapping to confirm non-erythroid origin.
- Radioimmunoassay and densitometry for quantification.
- Electron microscopy for binding site localization.
Main Results:
- Polypeptides (190-220 kDa) cross-reacting with erythrocyte ankyrin were found in pig brain membranes.
- Chymotrypsin cleavage yielded 95 kDa and 72 kDa fragments, similar to erythrocyte ankyrin fragments.
- The 72 kDa brain fragment bound to erythrocyte spectrin at the same site as erythrocyte ankyrin.
- Purified brain 72 kDa fragment showed distinct peptide maps from erythrocyte fragments.
- Brain ankyrin was estimated at 0.28% of membrane protein, similar to brain spectrin tetramer levels.
- The binding site on brain spectrin was localized to its midregion.
Conclusions:
- A protein closely related to erythrocyte ankyrin exists in brain membranes.
- This brain ankyrin likely functions as a membrane attachment site for brain spectrin, analogous to its role in erythrocytes.
- The findings support the conserved role of ankyrin in spectrin-cytoskeleton membrane attachment across different cell types.