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Measuring the peptides in individual organelles with mass spectrometry
New sampling protocols combined with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) allow the assay of single dense core vesicles. Understanding the packaging of vesicles is important as vesicles are the quanta of information for intercellular communicati...
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Published in: | Nature biotechnology 2000-02, Vol.18 (2), p.172-175 |
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creator | Sweedler, Jonathan V Rubakhin, Stanislav S Garden, Rebecca W Fuller, Robert R |
description | New sampling protocols combined with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) allow the assay of single dense core vesicles. Understanding the packaging of vesicles is important as vesicles are the quanta of information for intercellular communication. Using vesicles from the exocrine atrial gland of
Aplysia californica
as the model, a wide range of bioactive peptides are detected within each vesicle. Although the expression of the egg-laying hormone gene family of type 1 atrial gland cells has been previously examined, chemical characterization of individual 1–2 μm diameter vesicles demonstrates that products from several genes are colocalized. The mass sensitivity of MALDI MS can be further improved to enable the analysis of even smaller subcellular organelles. |
doi_str_mv | 10.1038/72622 |
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Aplysia californica
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Aplysia californica
as the model, a wide range of bioactive peptides are detected within each vesicle. Although the expression of the egg-laying hormone gene family of type 1 atrial gland cells has been previously examined, chemical characterization of individual 1–2 μm diameter vesicles demonstrates that products from several genes are colocalized. 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Understanding the packaging of vesicles is important as vesicles are the quanta of information for intercellular communication. Using vesicles from the exocrine atrial gland of
Aplysia californica
as the model, a wide range of bioactive peptides are detected within each vesicle. Although the expression of the egg-laying hormone gene family of type 1 atrial gland cells has been previously examined, chemical characterization of individual 1–2 μm diameter vesicles demonstrates that products from several genes are colocalized. The mass sensitivity of MALDI MS can be further improved to enable the analysis of even smaller subcellular organelles.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>10657123</pmid><doi>10.1038/72622</doi><tpages>4</tpages></addata></record> |
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subjects | Agriculture Animals Aplysia - chemistry Aplysia californica atrial gland Bioinformatics Biological and medical sciences Biomedical and Life Sciences Biomedical Engineering/Biotechnology Biomedicine Biotechnology Cytoplasmic Granules - chemistry Desorption Diverse techniques Electron microscopes Exocrine Glands - chemistry Fundamental and applied biological sciences. Psychology Genes Invertebrate Hormones - analysis Ionization Lasers Life Sciences Marine Mass spectrometry Microscopy Molecular and cellular biology Organelles - chemistry Packaging Peptides Peptides - analysis Scientific imaging Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods |
title | Measuring the peptides in individual organelles with mass spectrometry |
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