Measuring the peptides in individual organelles with mass spectrometry

被引:118
作者
Rubakhin, SS
Garden, RW
Fuller, RR
Sweedler, JV
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Univ Illinois, Beckman Inst, Urbana, IL 61801 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
dense-core vesicle; peptide; matrix-assisted laser desorption/ionization; Aplysia californica; atrial gland;
D O I
10.1038/72622
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 mu m 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.
引用
收藏
页码:172 / 175
页数:4
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