Relative quantitation of peptides in wild-type and Cpefat/fat mouse pituitary using stable isotopic tags and mass spectrometry

被引:63
作者
Che, FY [1 ]
Biswas, R [1 ]
Fricker, LD [1 ]
机构
[1] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10461 USA
来源
JOURNAL OF MASS SPECTROMETRY | 2005年 / 40卷 / 02期
关键词
peptide processing; carboxypeptidase E; neuropeptide; proopiomelanocortin; vasopressin; chromogranin;
D O I
10.1002/jms.742
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cpe(fat/fat) mice have a point mutation in the coding region of the carboxypeptidase E gene that renders the enzyme inactive. As a result, these mice have reduced levels of several neuropeptides and greatly increased levels of the peptide processing intermediates that contain C-terminal basic residues. However, previous studies examined a relatively small number of neuropeptides. In the present study, we used a quantitative peptidomics approach with stable isotopic labels to examine the levels of pituitary peptides in CPe(fat/fat) mice relative to wild-type mice. Pituitary extracts from mutant and wild type mice were labeled with the stable isotopic label [3-(2,5-dioxopyrrolidin-1-yloxycarbonyl)propyl]trimethylammonium chloride containing nine atoms of hydrogen or deuterium. Then, the two samples were pooled and analyzed by liquid chromatography/mass spectrometry (LC/MS). The relative abundance of peptides was determined from a comparison of the intensities of the heavy and light peaks. Altogether, 72 peptides were detected in the CPe(fat/fat) and/or wild-type mouse pituitary extracts of which 53 were identified by MS/MS sequencing. Several peptides identified in this analysis represent previously undescribed post-translational processing products of known pituitary prohormones. Of the 72 peptides detected in pituitary, 17 were detected only in the Cpe(fat/fat) mouse extracts; these represent peptide processing intermediates containing C-terminal basic residues. The peptides common to both Cpe(fat/fat) and wild-type mice were generally present at 2-5-fold lower levels in the Cpe(fat/fat) mouse pituitary extracts, although some peptides were present at equal levels and one peptide (acetyl beta-endorphin 1-31) was increased similar to7-fold in the Cpe(fat/fat) pituitary extracts. In contrast, acetyl beta-endorphin 1-26 was present at similar to10-fold lower levels in the Cpe(fat/fat) pituitary, compared with wild-type mice. The finding that many peptides are substantially decreased in Cpe(fat/fat) pituitary is consistent with the broad role for carboxypeptidase E in the biosynthesis of numerous neuropeptides. Copyright (C) 2005 John Wiley Sons, Ltd.
引用
收藏
页码:227 / 237
页数:11
相关论文
共 63 条
[1]   Family of hemorphins: co-relations between amino acid sequences and effects in cell cultures [J].
Blishchenko, EY ;
Sazonova, OV ;
Kalinina, OA ;
Yatskin, ON ;
Philippova, MM ;
Surovoy, AY ;
Karelin, AA ;
Ivanov, VT .
PEPTIDES, 2002, 23 (05) :903-910
[2]  
Bures EJ, 2001, PROTEOMICS, V1, P79, DOI 10.1002/1615-9861(200101)1:1<79::AID-PROT79>3.0.CO
[3]  
2-8
[4]   Cholecystokinin (CCK) levels are greatly reduced in the brains but not the duodenums of Cpe(fat)/Cpe(fat) mice: A regional difference in the involvement of carboxypeptidase E (Cpe) in pro-CCK processing [J].
Cain, BM ;
Wang, WG ;
Beinfeld, MC .
ENDOCRINOLOGY, 1997, 138 (09) :4034-4037
[5]   The SAAS granin exhibits structural and functional homology to 7B2 and contains a highly potent hexapeptide inhibitor of PC1 [J].
Cameron, A ;
Fortenberry, Y ;
Lindberg, I .
FEBS LETTERS, 2000, 473 (02) :135-138
[6]   Identification of peptides from brain and pituitary of Cpefat/Cpefat mice [J].
Che, FY ;
Yan, L ;
Li, H ;
Mzhavia, N ;
Devi, LA ;
Fricker, LD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) :9971-9976
[7]   Quantitation of neuropeptides in Cpefat/Cpefat mice using differential isotopic tags and mass spectrometry [J].
Che, FY ;
Fricker, LD .
ANALYTICAL CHEMISTRY, 2002, 74 (13) :3190-3198
[8]  
CHE FY, 2005, J MASS SPECTROM, V40
[9]   Missense polymorphism in the human carboxypeptlidase E gene alters enzymatic activity [J].
Chen, H ;
Jawahar, S ;
Qian, YM ;
Duong, QY ;
Chan, GY ;
Parker, A ;
Meyer, JM ;
Moore, KJ ;
Chayen, S ;
Gross, DJ ;
Glaser, B ;
Permutt, MA ;
Fricker, LD .
HUMAN MUTATION, 2001, 18 (02) :120-131
[10]   Cellular expression of isoforms of endothelin-converting enzyme-1 (ECE-1c, ECE-1b and ECE-1a) and endothelin-converting enzyme-2 [J].
Davenport, AP ;
Kuc, RE .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2000, 36 :S12-S14