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Protein Arrays (Biosurfaces for Proteome Research) Outline Protein Analysis – Introduction Why ? How ? New Protein Analysis Tools Protein Arrays SELDI MS – Based ProteinChip® Central Dogma of Life DNA mRNA Protection of DNA Amplification of genetic information Efficient regulation of gene expression Protein Proteins 20 amino acids 30,000 – 34,000 genes 2,000,000 proteins Protein Functions Signal transduction Transcription regulation Immune response Other vital cellular actions Proteomics An organism’s proteome: a catalog of all proteins expressed throughout life expressed under all conditions The goals of proteomics: to catalog all proteins to understand their functions to understand how they interact with each other Methods for Protein Analysis Gel electrophoresis, northern/western blot (fluorescence/radio active label) X-ray crystallography 2D - mass spectrometry Protein microarrays Antibody Array for Protein Expression Profiling Part1 Protein Microarray 1. High throughput analysis of hundreds of thousands of proteins. 2. Proteins are immobilized on glass chip. 3. Various probes (protein, lipids, DNA, peptides, etc) are used. Protein Array VS DNA Microarray Target: Binding: Stability: Surface: Printing: Amplification: Proteins (Big, 3D) 3D affinity Low Glass Arrayer Cloning DNA (Small, 2D) 2D seq High Glass Arrayer PCR Protein Array Fabrication Protein substrates Polyacrylamide or agarose gels Glass Nanowells Proteins deposited on chip surface by robots Benfey & Protopapas, 2005 Protein Attachment Diffusion Protein suspended in random orientation, but presumably active Adsorption/Absorption Some proteins inactive Covalent attachment Some proteins inactive Affinity Orientation of protein precisely controlled Diffusion Adsorption/ Absorption Covalent Affinity Benfey & Protopapas, 2005 Protein Interactions Different capture molecules must be used to study different interactions Examples Antibodies (or antigens) for detection Proteins for protein-protein interaction Enzyme-substrate for biochemical function Antigen– antibody Protein– protein Aptamers Enzyme– substrate Receptor– ligand Benfey & Protopapas, 2005 Expression Array Probes (antibody) on surface recognize target proteins. Identification of expressed proteins from samples. Typical quantification method for large # of expressed proteins. Interaction Array Probes (proteins, peptides, lipids) on surface interact with target proteins. Identification of protein interactions. High throughput discovery of interactions. Functional Array Probes (proteins) on surface react with target molecules . Reaction products are detected. Main goal of proteomics. Detection The preferred method of detection currently is fluorescence detection. The fluorescent detection method is compatible with standard microarray scanners, the spots on the resulting image can be quantified by commonly used microarray quantification software packages. However, some minor alterations to the analysis software may be needed. Other common detection methods include colorimetric techniques based on silver-precipitation, chemiluminescent and label free Surface Plasmon Resonance. Resources http://www.microarraystation.com/ Technical Challenges in Protein Chips 1. Poor control of immobilized protein activity. 2. Low yield immobilization. 3. High non-specific adsorption. 4. Fast denaturation of Protein. 5. Limited number of labels – low mutiplexing “Global Analysis of Protein Activities Using Proteome Chips” Snyder Lab, Yale University 2101-2105, Vol 293, Science, 2001 “Global Analysis of Protein Activities Using Proteome Chips” Snyder Lab, Yale University, 2101-2105, Vol 293, Science, 2001 Objectives 1.Construct yeast proteome chip containing 80% of yeast proteins in high throughput manner. 2.Study protein interactions at cell level using the proteome chip. “Global Analysis of Protein Activities Using Proteome Chips” Snyder Lab, Yale University, 2101-2105, Vol 293, Science, 2001 Protein Immobilization on Surface 1. Cloning of 5800 ORFs. 2. Production of fusion proteins (GST- HisX6). 3. Printing on glass chip. 4. Verification by anti-GST. “Global Analysis of Protein Activities Using Proteome Chips” Snyder Lab, Yale University, 2101-2105, Vol 293, Science, 2001 Protein-Protein Interactions 1. Calmodulin-Biotin with Ca++. 2. Interaction checked with Cy-3streptavidin 3. Six calmodulin targets newly found. 4. Another six known targets could not be detected. “Global Analysis of Protein Activities Using Proteome Chips” Snyder Lab, Yale University, 2101-2105, Vol 293, Science, 2001 Protein-Lipid Interactions 1. Phospholipids-Biotin. 2. About 150 proteins interacted with phospholipid probes. 3. Several of them were un-known, and some related to glucose metabolism. “Global Analysis of Protein Activities Using Proteome Chips” Snyder Lab, Yale University, 2101-2105, Vol 293, Science, 2001 Conclusions 1. Novel tool for protein interaction studies. 2. Concerns : * indirect interaction? * missing proteins? * surface chemistry? Antibody Array for Protein Expression Profiling http://www.youtube.com/watch?v=EeiN6beb CEw Part2 SELDI MS-based ProteinChip Utilizes Surface Enhanced Laser Desorption/Ionization Mass Spectrometry (1993) MALDI MS combined with chromatography (Bioaffinity): surfaceMALDI Protein Analysis by SELDI-MS 1 1) Apply sample (serum, tissue extract, etc.) to ProteinChip® array. 2 2) Wash sample with increasing stringency to remove non-specific proteins. 3) Energy absorbing molecules are added to retained proteins. Following laser desorption and ionization of proteins, Time-of Flight (TOF) mass spectrometry accurately determines their masses 3 Source:http://dir.niehs.nih.gov/proteomics/emerg3.htm Advantages & Applications of SELDI MS Extraction, fractionation, clean-up and amplification of samples on surface High throughput, high level multiplexing Large scale/ Low sample volume High sensitivity Various molecules on surface to capture probes Discover protein biomarkers Purification of target proteins Other fundamental proteomics research Mass Spectrometry Mass Spectrometry : Components 1. Ion source – sample molecules are ionized. Chemical, Electrospray, Matrix-assisted laser desorption ionization 2. Mass analyzer – ions are separated based on their masses. Time-of-flight, Quadruple, Ion trap 3. Mass detector 4. Data acquisition units Ion Sources Proteomics requires specialized ion sources Electrospray Ionization (ESI) With capillary electrophoresis and liquid chromatography Matrix-assisted laser desorption/ionization (MALDI) ESI MALDI Extracts ions from sample surface Benfey & Protopapas, 2005 Mass Analyzer Ion trap Captures ions on the basis of mass-to-charge ratio Often used with ESI Time of flight (TOF) Time for accelerated ion to reach detector indicates mass-tocharge ratio Frequently used with MALDI Also other possibilities Ion Trap Time of Flight Detector Benfey & Protopapas, 2005 Mass Spectrometry for Proteins 1. ESI-Ion Trap Sample in solution, lower mass limit. 2. MALDI-TOF Solid state measurement, high mass limit, most popular tool for protein analysis. Protein Identification by MS Preparation of protein sample Extraction from a gel Digestion by proteases — e.g., trypsin Mass spectrometer measures mass-charge ratio of peptide fragments Identified peptides are compared with database Software used to generate theoretical peptide mass fingerprint (PMF) for all proteins in database Match of experimental readout to database PMF allows researchers to identify the protein Mass Spectrum of Protein mixture Advantages of Mass Spectrometry 1. No labeling required. 2. Fast separation. 3. Multiplexing feasibility. 4. High sensitivity. Disadvantages of Mass Spectrometry 1. Lower sensitivity compared to array. 2. Lower accuracy in quantitative assay. 3. Stringent sample purity. “SELDIProteinChip Array Technology: Protein-Based Predictive Medicine and Drug Discovery Applications” Ciphergen Biosystems, Inc, 237-241, Vol 4, J. Biomed. & Biotechnol., 2003 “SELDIProteinChip Array Technology: Protein-Based Predictive Medicine and Drug Discovery Applications” Ciphergen Biosystems, Inc, 237-241, Vol 4, J. Biomed. & Biotechnol., 2003 SELDIProteinChip Array Technology 1. ProteinChip Array, ProteinChip Reader, asso. software 2. Surface: hydrophobic, hydrophilic, ion exchange, metal-immobilized, etc… 3. Probes (baits): antibodies, receptors, oligonucleotides 4. Samples: cell lysates, tissue extracts, biological fluids “SELDIProteinChip Array Technology: Protein-Based Predictive Medicine and Drug Discovery Applications” Ciphergen Biosystems, Inc, 237-241, Vol 4, J. Biomed. & Biotechnol., 2003 Application 1: Identification of HIV Replication Inhibitor 1. CAF (CD8+ antiviral factor) though to be related to AIDS development 2. Determined the identity of CAF with SELDI techniques : alpha-defensin -1, -2 and -3 3. Demonstrated de novo discovery of biomarker and multimarker patterns, identification of drug candidates and determination of protein functions “SELDIProteinChip Array Technology: Protein-Based Predictive Medicine and Drug Discovery Applications” Ciphergen Biosystems, Inc, 237-241, Vol 4, J. Biomed. & Biotechnol., 2003 Application 2: Multimarker Clinical Assays for Cancer 1. Early detection of cancer – critical in effective cancer treatment 2. Cancer biomarker – massive protein expression profiling 3. High throughput assay for multimarker provided by SELDI array and multivariate software algorithms produced high sensitivity and specificity. “SELDIProteinChip Array Technology: Protein-Based Predictive Medicine and Drug Discovery Applications” Ciphergen Biosystems, Inc, 237-241, Vol 4, J. Biomed. & Biotechnol., 2003 Application 3: Biomarker and Drug Discovery Applications in Neurological Disorders 1. SELDIProteinChip for Alzheimer’s Disease 2. Wide rage of samples Small sample amount 3. SELDI using antibody protein array : Ab against Nterminal sequence of target peptides (beta-amyloid) 4. Discovered candidate biomarkers, related inhibitors, & their functions and peptide expression levels