Quantification of p38/synaptophysin in highly purified adrenal medullary chromaffin vesicles
- 6 June 1988
- journal article
- Published by Wiley in FEBS Letters
- Vol. 233 (1) , 22-24
- https://doi.org/10.1016/0014-5793(88)81348-6
Abstract
Chromaffin vesicles were first purified by differential and density gradient centrifugation in isotonic (Percoll) gradients. In subsequent sucrose gradients p38/synaptophysin exhibited the same distribution as established marker substances of chromaffin vesicles. Quantification of immunoblots revealed that 750 ng p38/synaptophysin per mg of protein were present in the chromaffin vesicles recovered from the sucrose gradient. Thus the amount of p38/synaptophysin per mg protein of chromaffin vesicles is about 100 times lower than that observed in clear (synaptic) vesicles. However, because of the large difference in surface area and protein content, the amount of p38/synaptophysin per single vesicle is the same in both types of organellesKeywords
This publication has 12 references indexed in Scilit:
- Endocrine secretory granules and neuronal synaptic vesicles have three integral membrane proteins in common.The Journal of cell biology, 1988
- Cloning and sequence analysis of cDNA encoding p38, a major synaptic vesicle protein.The Journal of cell biology, 1987
- A Synaptic Vesicle Protein with a Novel Cytoplasmic Domain and Four Transmembrane RegionsScience, 1987
- Protein p38: an integral membrane protein specific for small vesicles of neurons and neuroendocrine cells.The Journal of cell biology, 1986
- Identification and localization of synaptophysin, an integral membrane glycoprotein of Mr 38,000 characteristic of presynaptic vesiclesCell, 1985
- A 38,000-dalton membrane protein (p38) present in synaptic vesicles.Proceedings of the National Academy of Sciences, 1985
- Distribution of chromaffin secretory vesicles, acetylcholinesterase, and lysosomal enzymes in sucrose and percoll gradientsAnalytical Biochemistry, 1984
- Latent acetylcholinesterase in secretory vesicles isolated from adrenal medullaBiochimica et Biophysica Acta (BBA) - Biomembranes, 1981
- Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proceedings of the National Academy of Sciences, 1979
- Proteins and Sodium Dodecyl Sulfate: Molecular Weight Determination on Polyacrylamide Gels and Related ProceduresPublished by Elsevier ,1975