Identification of mouse brain neuropeptides by high throughput mass spectrometry

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594 生物工程学报 Chinese Journal of Biotechnology http://journals.im.ac.cn/cjbcn DOI: 10.13345/j.cjb.170361 生物技术与方法 邵先锋等 / 高通量质谱法用于小鼠脑部神经肽的鉴定 Apr. 25, 2018, 34(4): 594 601 2018 Chin J Biotech, All rights reserved 邵先锋 1,2, 马敏 2,3, 陈瑞冰 1, 贾辰熙 2 1 300070 2 102206 3 300072,,,.., 2018, 34(4): 594 601. Shao XF, Ma M, Chen RB, et al. Identification of mouse brain neuropeptides by high throughput mass spectrometry. Chin J Biotech, 2018, 34(4): 594 601. 摘要 : 神经肽在参与调控人体各种生理功能上发挥着重要的作用, 如痛觉 睡眠 情绪 学习与记忆等生理活动都受到神经肽的影响 神经肽主要存在于机体的神经组织内, 其他体液和器官中也有少量的分布 目前对全脑组织神经肽高通量鉴定的研究仍不足, 高通量检测这些神经肽对了解神经肽的组成和功能具有重要的意义 本研究通过对小鼠全脑组织内源性肽段的萃取, 运用液相串联质谱 (LC-MS/MS) 技术对全脑组织的神经肽进行检测, 共鉴定到 1 830 条内源性肽段和 99 条预测神经肽肽段 这些内源性肽段的鉴定在疾病的治疗和机制研究以及药物的研发方面提供了参考价值, 也为研究新的神经肽及其功能奠定了基础 : 神经肽, 全脑组织, 高通量鉴定, 内源性肽段, 液相串联质谱 Identification of mouse brain neuropeptides by high throughput mass spectrometry Xianfeng Shao 1,2, Min Ma 2,3, Ruibing Chen 1, and Chenxi Jia 2 1 School of Basic Medicine, Tianjin Medical University, Tianjin 300070, China 2 Beijing Institute of Radiation Medicine, State Key Laboratory of Proteomics, Beijing Proteome Research Center, National Center for Protein Sciences-Beijing, Beijing 102206, China 3 School of Life Sciences, Tianjin University, Tianjin 300072, China Abstract: Neuropeptides play an important role in the physiological functions of the human body. The physiological activities such as pain, sleep, mood, learning and memory are affected by neuropeptides. Neuropeptides mainly exist in the nerve tissue of the body, and a small amount of them are distributed in body fluid and organs. At present, analysis of large-scale identification Received: September 15, 2017; Accepted: November 7, 2017 Supported by: National Key Research and Development Program of China (No. 2016YFA0501302), National Natural Science Foundation of China (No. 21675006). Corresponding authors: Chenxi Jia. E-mail: cjia@mail.ncpsb.org Ruibing Chen. E-mail: chenruibing@tijmu.edu.cn (No. 2016YFA0501302) (No. 21675006) 2017-11-21 http://kns.cnki.net/kcms/detail/11.1998.q.20171121.1110.002.html

邵先锋等 / 高通量质谱法用于小鼠脑部神经肽的鉴定 595 of neuropeptides in whole brain tissue is still challenging. Therefore, high-throughput detection of these neuropeptides is greatly significant to understand the composition and function of neuropeptides. In this study, 1 830 endogenous peptides and 99 novel putative neuropeptides were identified by extraction of endogenous peptides from whole brain tissue of mice by liquid phase tandem mass spectrometry (LC-MS / MS). The identification of these endogenous peptides provides not only a reference value in the treatment and mechanism studies of diseases and the development of drugs, but also the basis for the study of a new neuropeptides and their functions. Keywords: neuropeptides, whole brain tissue, high-throughput detection, endogenous peptides, LC-MS/MS 10 30 Orbitrap Fusion 3 Western blotting [1-3] [4-6] [7-9] [10] 1 材料与方法 1.1 小鼠全脑组织标本的采集 8 SPF C57BL/6 (30 40 g) (22±1) 65% 70% 1 9 CO 2 5 min PBS 3 750 W 30 s 80 1.2 神经肽的提取 2 3 ( 1) 1M (Methanol) l ml (90% 1% ) 2 min 4 20 000 g 10 min 0.1% 4 20 000 g 10 min 1/2 C18 (Agilent USA) 45% (45% 0.1% ) 80 2MF (Methanol & 010-64807509 cjb@im.ac.cn

596 ISSN 1000-3061 CN 11-1998/Q Chin J Biotech 图 1 小鼠全脑神经肽的提取流程 Fig. 1 The extraction process of mouse total cerebral neuropeptides. Filter) l ml 30 kda (Millipore UFC5030BK USA) 14 000 g 8 min 3 0.1% 4 14 000 g 40 min 200 μl 0.1% 30 min 1/2 1.3 LC-MS/MS 的设定 Thermo EASY-nLC1200 (Thermo Fisher Scientific Bremen Germany) 20 μl 0.1% 700 ng C18 ( 3 μm 120 Å) (SunChrom, USA) B (0.1% 80% ) C18 ( 75 mm 15 cm) 0 min-7% B 14 min-13% B 51 min-23% B 68 min-36% B 69 min-100% B 75 min-100% B 600 nl/min Thermo orbitrapfusion (Thermo Fisher Scientific Bremen Germany) 120 000 5.0 e5 50 ms 300 1 400 m/z 2.0 e5 35 ms 1.6 m/z 120 m/z 30% 18 s +1 >+6 2 数据的处理 PEAKS Studio (Version8.5) [11] 10 Da 0.2 Da FDR 1% 10 logp 20 Amidation Oxidation (M) Phosphorylation (STY) Acetylation (K) 2 (1) swepep peptides [12] (http://www.swepep.org/) neuropedia [13] (http://proteomics.ucsd.edu/software/ NeuroPedia/) neuropep [14] (http://isyslab.info/neuro Pep/) (2) neuropred [15] (http://stagbeetle.animal.uiuc.edu/cgi-bin/neuropred.py) swepep predicted (http://www.swepep.org/) (3) swepep precursors (http:// www.swepep.org/) http://journals.im.ac.cn/cjbcn

邵先锋等 / 高通量质谱法用于小鼠脑部神经肽的鉴定 597 3 结果与分析 3.1 数据库的优化 MF (1) 3 swepep neuropedia neuropep 1 392 976 1 167 swepep 1 269 ( 2) 3 neuropedia 894 neuropep 1 070 swepep neuropedia 67.5% neuropep 71.2% neuropedia swepep 78.7% swepep 279 neuropep 12 9 (Somatostatin) B (Proenkephalin-B) (POMC) 1 (PPT) (CCK) (Pro-TRH) 2 (SCG2) - (Cocaine-and amphetamine-regulated 图 2 不同数据库鉴定到的内源性肽段数 Fig. 2 The identification number of endogenous peptides by using different databases. transcript protein) (GRP) 3 3.2 不同制样方法的鉴定结果 M MF 2 1 486 1 453 2 1 361 1 326 ( 1) 2 3 P (SP) B K Y (NPY) (VIP) SP [16-17] NPY [18] [19-20] VIP 3 0.76 ( 3A) M MF 993 895 ( 3B) 2 7 kda 30 kda 2 M MF 64.1% ( 4A) M 311 B -14 B [21] -14 [22] MF 276 K ( 010-64807509 cjb@im.ac.cn

598 ISSN 1000-3061 CN 11-1998/Q Chin J Biotech [23] ) A (1-8) ( ) 2 1 830 1 653 1 653 6 30 95.6% ( 4B) 11 15 640 38.7% 5 60 SCG1 表 1 两种样品制备方法的内源性肽段的鉴定 Table 1 The identified endogenous peptides from two different sample preparation methods Group Identified peptides Max mass Amidation Oxidation Phosphorylation Acetylation M 1 486/1 361 6 979 72 47 82 71 MF 1 453/1 326 6 194 77 58 79 79 图 3 皮尔森系数和内源性肽段的鉴定数 Fig. 3 The Pearson coefficient and the number of identified endogenous peptides. M1 3: samples from the methanol group; MF1 3: samples from the methanol & filter group. (A) The Pearson coefficient among 6 samples. (B) The number of identified endogenous peptides of different samples. 图 4 内源性肽段的鉴定数及氨基酸的长度 Fig. 4 The number of identified endogenous peptides and their amino acid length. (A) Recurrence rate of endogenous peptides between the M group and the MF group. (B) The amino acid lengths of peptides identified in 6 samples. http://journals.im.ac.cn/cjbcn

邵先锋等 / 高通量质谱法用于小鼠脑部神经肽的鉴定 599 3.3 前体荷尔蒙的鉴定 neuropred [15] (3) 2 176 1 941 100 SCG2 1 (PEBP-1) SCG1 Ⅰ (ProSAAS) ( 5) 4 49.5% 3.4 对新神经肽的探索 (2) 2 (2) 99 42 SCG2 6 A ( 2) VIP peptides ISSSISEDPVPI mrna A YGGFMR YGGFMRSL 图 5 前体荷尔蒙的分布 Fig. 5 The distribution of precursor hormones. SCG2: Secretogranin-2; PEBP1: phosphatidyle thanolaminebinding protein 1; PCSK1: prohormone convertase 1; PENK: proenkephalin-a; TYB4: thymosin beta-4; POMC: Pro-opiomelanocortin; 7B2: neuroendocrine protein 7B2; CCKN: cholecystokinin. 表 2 部分预测肽段的信息 Table 2 The information of several predictive peptides Peptide sequences 10 lg (P value) Gene names Protein names YGGFMR 31.13 PENK Proenkephalin-A PKLKWDNQ 43.40 PDYN Proenkephalin-B YGGFMRSL 49.40 PENK Proenkephalin-A SEESQEREY 56.07 CHGB Secretogranin-1 ISSSISEDPVPI 40.25 VIP VIP peptides RPKPQQFFGLMG 60.71 TAC1 Protachykinin-1 APGAMLQIEALQEVLKKL 61.74 CARTPT Cocaine- and amphetamine-regulated transcript protein WSRMDQLAKELTAE 59.79 CHGA Chromogranin-A ILTGSSEPEAAPAPR 54.22 PCSK1N ProSAAS 010-64807509 cjb@im.ac.cn

600 ISSN 1000-3061 CN 11-1998/Q Chin J Biotech 4 讨论 CRF ACTH UCN AVP VIP CCK [24-26] M 993 MF 98 M LTQ Orbitrap Discovery 500 [27] [28] swepep neuropedia neuropep 80% swepep neuropedia 37 612 37 / 125 20.4% 110 18.0% [29] [30] SCG2 SCG2 [28] SCG2 PENK 215 88 SCG2 PENK SCG2 PENK 41 102 REFERENCES [1] Sharma K, Schmitt S, Bergner CG, et al. Cell type- and brain region-resolved mouse brain proteome. Nat Neurosci, 2015, 18(12): 1819 1831. [2] Petruzziello F, Falasca S, Andren PE, et al. Chronic nicotine treatment impacts the regulation of opioid and non-opioid peptides in the rat dorsal striatum. Mol Cell Proteomics, 2013, 12(6): 1553 1562. [3] Che FY, Lim J, Pan H, et al. Quantitative neuropeptidomics of microwave-irradiated mouse brain and pituitary. Mol Cell Proteomics, 2005, 4(9): 1391 1405. [4] Chen RB, Xiao MM, Buchberger A, et al. Quantitative neuropeptidomics study of the effects of temperature change in the crab Cancer borealis. J Proteome Res, 2014, 13(12): 5767 5776. [5] Molina FA, Burrows NP, Jones RR, et al. Increased sensory neuropeptides in nodular prurigo: a quantitative immunohistochemical analysis. Br J Dermatol, 1992, 127(4): 344 351. [6] Doughty SE, Atkinson ME, Shehab SAS. A quantitative study of neuropeptide immunoreactive cell bodies of primary afferent sensory neurons following rat sciatic nerve peripheral axotomy. Regul Pept, 1991, 35(1): 59 72. [7] Gouardères C, Quelven I, Mollereau C, et al. Quantitative autoradiographic distribution of NPFF 1 neuropeptide FF receptor in the rat brain and comparison with NPFF 2 receptor by using [ 125 I]YVP and [( 125 I]EYF as selective radioligands. Neuroscience, 2002, 115(2): 349 361. [8] de Dreu CKW, Greer LL, Handgraaf MJJ, et al. The neuropeptide oxytocin regulates parochial altruism in intergroup conflict among humans. Science, 2010, 328(5984): 1408 1411. http://journals.im.ac.cn/cjbcn

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