4疾病蛋白质组学.ppt

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1、第四讲 疾病蛋白质组学（一）disease proteomics,一、基本概念和总体研究概况,疾病蛋白质组学disease proteomics,运用蛋白质组学研究手段，通过比较正常和病理情况下细胞、组织或体液中蛋白质在组成成分、表达水平、表达位置和修饰状态上的差异，寻找疾病诊断和预后的特异性蛋白质(群)，包括特异性抗原及相关抗原、受体、酶等，以及药物治疗的靶标等。通过深入了解这些疾病特异性蛋白质的结构和功能，揭示疾病过程中细胞内全部蛋白质的活动规律，为多种疾病发生、发展机制的阐明和早期诊断及治疗提供理论根据和解决途径。,研究进展,肿瘤蛋白质组：研究细胞的增殖、分化、异常转化、肿瘤形成白血病、

2、乳腺癌、结肠癌、膀胱癌、前列腺癌、肺癌、肾癌、肝细胞癌和神经母细胞瘤等联合激光捕获微切割技术(Laser capture mierodisseetion，LCM)，直接从肿瘤组织中提取纯肿瘤细胞，以克服组织内异质性的问题，为肿瘤蛋白质组研究提供了技术上的保障。鉴定了一批肿瘤相关蛋白，为肿瘤的早期诊断、药靶的发现、疗效和预后的判断提供了重要依据。在心脏、肺部、内分泌系统、神经系统疾病、药物成瘾性、环境毒理学、传染病、内耳相关疾病等方面，蛋白质组研究成果也为其提供了新的诊疗方向。国内：重点在肝病、恶性肿瘤、心血管、神经系统疾病和新发传染病等方面,存在问题和发展趋势,利用蛋白质组研究的人类疾病的范围

3、虽然日趋扩大，但仍停留在初级比较阶段。进一步鉴定、验证，发展成应用于临床的生物标志物开展全方位的蛋白质组相互作用网络的分析进一步提高蛋白分离和鉴定的通量、灵敏度和规模；提高生物信息学应用范围与准确率，进行信息综合，准确地分析蛋白质的相互作用，界定相互作用连锁群；,二、心血管疾病蛋白质组学 Cardiovascular Proteomics,the cardiovascular(CV)system is composed of a number of specialized cell types including cardiac myocytes,fibroblast,neurons,endo

4、thelial and smooth muscle cells and newly discovered stem and progenitor cells.To date,the proteome of these cells are not well characterized nor has the interplay between the cell types been established in health or disease.This remains a significant challenge as CV disease is the number one killer

5、 world wide.,Research Focus,The myofilament proteome.Redox modifications in the cardiac proteome.Cardiac biomarkers.Secretory microvesiclesProteomics of the secretome,The myofilament proteome,The myofilament（肌丝）proteins are responsible for the contractile nature of the cardiac myocytes.the myofilame

6、nt subproteome allows the heart to act as a pump.The myofilament proteins are highly regulated by a number of specific post-translational modifications(PTMs)some of which have been discovered through proteomic studies.PTMs of myofilament proteins can directly impact on the contractility of the heart

7、.,A simplified illustration of the cardiac myofilament proteins.The thick filament proteins consist of myosin heavy chain(MHC),myosin-binding protein C(MyBP-C),and two myosin light chains(MLC1 and MLC2).The thin filament proteins consist of actin,tropomyosin(Tm),and the three components of troponin;

8、troponin I(TnI),troponin C(TnC)and troponin T(TnT).Phosphorylation sites on the myofilament proteins are indicated with a small diamond.The large scaffolding protein,titin,which spans the sarcomere,is not included in this illustration.,肌球蛋白重链(MHC):myosin heavy chain肌球蛋白轻链-1,2(MLC1,2):myosin light ch

9、ain-1,2肌动蛋白：Actin肌球蛋白结合蛋白C(MyBP-c):myosin binding protein C）肌钙蛋白(TnT,TnI,TnC):troponin T,I，C-原肌球蛋白(Tm)：-tropomyosin肌联蛋白:titin,Structure of a region of the overlap region of a cardiac sarcomere in diastole on the left and during systole on the right with indications of major and functionally signific

10、ant protein phosphorylation sites.,Post-translational modifications of myofilament proteins,Sample preparation,There are two commonly used myofilament protein-enrichment strategies.Both methods are compatible with 1-DE and 2-DE analysis：TFA(trifluoroacetic acid,三氟醋酸)extraction：cells are lysed with l

11、ow ionic buffer,and myofilament proteins are extracted from the resulting pellet with 1%TFA v/v.applied to extract myofilament proteins from minute amounts(20,50 mg)of biopsy samples.（ref:Proteomics 2002,2,978987.)Myofibril isolation：intact myofibrils can be isolated form detergent-skinned(detergent

12、 extraction)heart muscle and stored in 50%glycerol at-20 C.(ref:FASEB J.2005,19,11371139.),Detection Methods for Protein modification,phosphorylation changes:1-D-IEF(phosphorylation significantly decreases protein pI values)Western blots with phosphorylation-site-specific antibodies MS analysis:MALD

13、I-TOF coupled with phosphatase treatment or Post source decay(PSD)immobilized metal affinity column(IMAC)enrichment and LC separation followed by MS/MS analysis,Immobilized metal affinity column(IMAC),Schematic of affinity binding of phosphopeptides to immobilized metal ion affinity columns.,Detecti

14、on Methods for Protein modification,Protein degradation:1-D-gel separation followed by Western blot2-DE,2-D DIGEdirect sequencing from the N terminus or MS(exact site of degradation)oxidation and nitrosylation:gel electrophoresis(change apparent MWand pI values)nano-ESI LC/MS/MS(identify nitrotyrosi

15、ne residues)“top-down”MS(傅里叶转换离子回旋共振质谱）,文献阅读,Proteomics Clin.Appl.(2008)Chao Yuan,R.John Solaro.Myofilament proteins:From cardiac disorders to proteomic changes(p 788-799)Wenhai Jin,Anna T.Brown,Anne M.Murphy.Cardiac myofilaments:from proteome to pathophysiology(p 800-810),2.Redox modifications in t

16、he cardiac proteome,Myocardial ischemia results in oxidative stress,which involves the mitochondria and many/all aspects of myocyte function.Due to the susceptibility of cardiac protein to oxidative damage,proteomics can help to discover,quantify,and characterize the redox signaling and oxidative PT

17、Ms.Nitric oxide is a key mediator of CV cellular response in acute and chronic disease settings.New approaches in the proteomics can help identify and define important pathway of nitric oxide-induced PTMs.,Outline of potential consequences of oxidative stress in cell system,Oxidants can react with p

18、roteins to cause one of two broad consequences.They can oxidise cellular components such as proteins,rendering them dysfunctional,which negatively affects cell function and promotes disease.In this scenario,antioxidants can prevent the cellular proteins from being oxidised and so provide protection.

19、In contrast,oxidants can induce regulatory post-translational oxidative protein modifications,which are important for stress adaptation.Thus,antioxidants can interfere with homeostatic control and might explain why antioxidant therapies can be detrimental in some cases.,Mechanisms of ROS generation.

20、Sequential reduction of molecular oxygen to generate superoxide,hydrogen peroxide and then hydroxyl radical.List of amino acids particularly susceptible to modification.,Diagram showing the production of NO and RNS,with their effects on biological targets.At high concentrations,NO reacts mainly with

21、 oxygen superoxide forming peroxynitrite(ONOO)and peroxynitrous acid(ONOOH).In this way,NO is intimately linked with ROS.Moreover,the reaction of NO with O2 leads to the formation of the highly poisonous nitrogen dioxide(NO2),dinitrogen tetroxide(N2O4),or both.At low concentrations,the direct effect

22、s of NO predominate(dashed arrow)and haems and redox metals at ironsulphur centres in proteins are the main targets.Ni-NOR,nitrite:nitric oxide reductase;Ni,nitrite reductase;NOS,nitric oxide synthase;NR,nitrate reductase;RSNOs,S-nitrosothiols.,Structure of common redox modifications of amino acid s

23、ide chains.ROS and RNS can chemically modify amino acids,particularly the side chains of those outlined here.Clearly,cysteine thiols are subject to a diverse range of alterations.,亚磺酸,磺酸,次磺酸,亚砜,亚硝基硫醇,羰基化,硝基化酪氨酸,Commonly observed oxidative modifications of protein amino acids(A)cysteine;(B)methionine

24、;(C)tyrosine;(D)tryptophan.All the amino acids are schematically represented as part of a polypeptide chain.However,the names shown are those of free amino acids for convenience.,List of the most utilized methods in redox proteomics,Biotin switch method A hypothetical protein is indicated with cyste

25、ines in either the free thiol,disulphide,or nitrosothiol conformations.In the first step,free thiols are blocked using MMTS.Next,nitrosylated cysteine residues are selectively reduced with ascorbate and the newly generated free thiols are finally S-biotinylated with biotin-HPDP.,The biotinylated pro

26、teins can be detected directly by Western blotting with antibodies specific for biotin or using avidin or streptavidin.Antibodies can be radiolabelled,fluorescently or enzymatically labelled,as is known in the art.Additionally,tagged proteins can also be isolated from affinity columns or beads.PSH,p

27、rotein sulphhydryl groups;PSNO,Snitrosated proteins.,Isotope Coded Affinity Tagging(ICAT)(a).The reagent consists of three moieties:an affinity tag biotin,a linker that can incorporates stable isotopes,and a maleimide(顺丁烯二酰亚胺)group which reacts specifically with the thiol group of cysteine.Two label

28、led forms of the reagent are used,the heavy containing eight deuteriums(氘)and the light with none.,(b)Proteins from two different cell states are labelled with the light or heavy ICAT reagents.The samples are then combined and digested.The ICAT-labelled peptides are isolated by affinity chromatograp

29、hy using an avidin column and then analysed HPLC-MS(/MS)directly or by MALDI of the collected HPLC fractions.The ratio of the peaks areas for specific ICAT-labelled pairs defines the relative abundance of its parent proteins between the two cell states,quantification of protein cysteineoxidation,Lis

30、t of cardiac proteins demonstrated to undergo oxidative modification,Ref:Proteomics Clin.Appl.2008,2,823836,3.Cardiac biomarkers,Diagnosis of MI relies on the detection in serum of a cardiac specific isoform of the myofilament protein,troponin I which is released into the blood when the cardiac myoc

31、yte dies due severe ischemiaEarlier detection of MI or diagnosis of myocardial ischemia prior to cell death will help to allow even earlier intervention to save“potentially viable”heart muscle.proteomic discovery pipeline for analysis of human plasma samples for patients with induced and control MI

32、helped to set the stage for earlier detection of patents at high risk.,Current gold standard markers of CV distress,(i)electrophysiological and functional changes as monitored by electrocardiography and echocardiography respectively(ii)elevated serum levels of cardiac specific proteins：myofilament p

33、roteins and cardiac troponin-I and-T（myocardial infarction）brain natriuretic peptide and inflammation-related proteins,including C-reactive protein(CRP),（heart failure）.cardiac enzymes lactate dehydrogenase and creatine kinase(CK),Several approaches currently used to quantitativelyprofile global pro

34、teomic expression patterns,fluorescence 2-D DIGE coupled to MS analysisProtein arraysin vitro and in vivo stable isotope label LC-MS techniques Significant cost of using labeled reagents in large-scale studies.the apparent bias of these techniques towards labeling the relatively most abundant specie

35、s in a complex mixture,More recently,“label-free”differential(d)MS(无标记的质谱定量方法),Workflow for label-free dMS analysis of plasma samples.(A)Workflow chart.The six stages of the process are represented within this figure including sample preparation,addition of internal standards and MS analysis.Each st

36、age plays an important role in leading to a successful of determination of meaningful differentials.,4.Secretory microvesicles,Vascular secretory protein and membrane vesicles can affect homeostasis and communication within entire CV system in response to injury.,Schematic figure of the use of prote

37、omics for the characterization of the non-cellular protein fractions relevant in atherosclerosis.The figure represents an atherosclerotic plaque and its cellular components.The cells involved in atheroma formation release soluble proteins and membrane bodies that modify the vascular microenvironment

38、.Proteomics can be applied to the characterization of these non-cellular components of the atherosclerotic microenvironment.,The limitations of plasma proteomics,plasma and serum are routinely used for biomarker discovery in proteomics.the high-abundance proteins,notably albumin and immunoglobulins,

39、which together with haptoglobulin,antitrypsin and transferrin,typically constitute more than 90%of the total protein mass in human plasma.prospective biomarkers:pgng/ml;albumin:3550 mg/mlthe limited ability of proteomics to detect low-abundance plasma proteins,Proteomics of extracellular secretoryve

40、sicles,(3)Matrix vesicles are extracellular membrane particles observed in the initial stages of arterial calcification and contain high levels of calcium-binding acidic phospholipids.(4)Apoptotic bodies are large particles released from cells at the later stages of programmed cell death and charact

41、erized by large diameter,nuclear content,and surface ligands for phagocytic cell receptors.(5)Heterogeneous population or secretory microvesicles.,(1)Microparticles are released from the plasma membrane of stimulated or apoptotic cells.Their protein composition may vary in response to different stim

42、uli(high shear stress,apoptosis,etc.).(2)Exosomes are the smallest of the secretory membrane particles and are secreted as a consequence of the fusion of the plasma membrane with the multivesicular bodies(MVB).MVB are late components of the endocytic pathway.,The critical patho-physiological role of

43、 microparticles,In the vascular context,microparticles are released by endothelial cells,smooth muscle cells,lymphocytes,monocytes,erythrocytes and platelets.Plasma levels of microparticles are markedly elevated in patients with vein thrombosis,acute coronary disease,ischemic stroke,diabetes,myocard

44、ial infarction,and hypertension.Microparticles show pro-coagulant activity,pro-inflammatory,and pro-atherosclerotic activities.modulating the endothelial secretion of prostacyclin and nitric oxide;promote monocyte-endothelium interaction by direct transfer of arachidonic acid to the plasma membrane;

45、physically mediate leukocyte-leukocyte and leukocyte-endothelium interactions via direct binding of cell surface receptors,Proteomics of microparticles,Proteomic analysis of protein expression in human plasma microparticles.Microparticles derived from the peripheral blood by centrifugation were lyse

46、d and labelled with Cydyes(green and red colour in A and B,respectively).Using DIGE,microparticle and microparticle-depleted plasma proteins were co-separated in large format 2-D gels.Images were acquired on a fluorescence scanner and proteins identified by LC-MS/MS.Actin and haemoglobin are enriche

47、d in microparticles,compared to microparticle-depleted plasma.,characterisation of microparticles released by a particular cell type in vitro by proteomics,Besides the investigation of the mixture of microparticles contained in human plasma,proteomics can be applied to the characterisation of microp

48、articles released by a particular cell type in vitro.platelet microparticles(J.Proteome Res.2005;4:15161521)surface proteins typical of platelets,such as integrin aIIb,integrin b3 and P-selectin,and chemokines,such as CXCL4,CXCL7 and CCL5,380 proteins not previously identified in plateletsEndothelia

49、l cells in response to stimulation with(TNFa).(Proteomics 2005;5:44434455)cytoskeleton and cytoskeleton-binding proteins(tubulin,actin,cofilin,vimentin,etc.)membrane-associated proteins that control transport and signalling(caveolin,annexins,dynein,etc.)foldingchaperones(calnexin,calreticulin,etc.)A

50、dhesion molecules,such as ICAM-1 and integrins b1,a5 and a2,The role of Exosomes,modulate immune responseregulate haemostatic balancesupport thrombin generation and induce expression and secretion of plasminogen activator inhibitor-1 by endothelial cellsattenuating fibrinolysis and promoting pro-thr