Total Protein Measurement methods. Human proteins – More than 50,000 Within one cell 3000 to 5000...
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Transcript of Total Protein Measurement methods. Human proteins – More than 50,000 Within one cell 3000 to 5000...
![Page 1: Total Protein Measurement methods. Human proteins – More than 50,000 Within one cell 3000 to 5000 Serum – More than 1400 different proteins.](https://reader036.fdocuments.us/reader036/viewer/2022081515/56649e4e5503460f94b448ce/html5/thumbnails/1.jpg)
Total Protein
Measurement methods
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• Human proteins– More than 50,000
• Within one cell 3000 to 5000• Serum – More than 1400 different proteins
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Interim Consensus Reference Intervals for 14 Plasma Proteins In Human Serum
*Values are slightly lower in fresh samples (assayed <8 hr after draw)
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• Distribution – Vascular,extravascular space– Kind and proportions of individual proteins • Molecular size • Specificity of some of their transport mechanisms • Disease
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Plasma proteins
• Alterations of plasma proteins – Genetic origin– Physiological – Pathological • Clinical findings • Technical
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Plasma proteins
• Patient ’s endocrine status – Rates of hepatic synthesis – Steroid hormones
• Inflammatory acute-phase reaction• Mask effect
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• Increased Plasma Levels – acute dehydration
• no clinical utility • Synthetic rate and intravascular—extravascular shifts
• Decreased Plasma Levels – Decreased synthesis
• Primary or genetic – Analbuminemia
• Acquired – Inflammatory processes
– Increased catabolism • Utilization or loss
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ANALYSIS OF PROTEINS Methods
• Specific quantitative assays (Individual proteins)
– Immunochemical methods • Nephelometry • Turbidimetry • RID • Electroimmunoassay • RIA or enzyme immunoassay (EIA)
– very low concentrations
• Detection and identification – Electrophoresis
• Quantitative measurements of total protein
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ANALYSIS OF PROTEINS Methods
• Nephelometric and turbidimetric – Speed and ease– Formation of Ag-Ab complex– Light absorption & scattering
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Assay Characteristics
• Limit of Detection – nephelometric methods• 10 µg/mL
– turbidimetric methods • 20 to 30 µg/mL
– RID methods • 10 to 20 µg/mL
– RIA methods• nanograms per milliliter
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Assay Characteristics
• Precision – Nephelometry and turbidimetry• within-run coefficients of variation (CVs) of less than
5% • equilibrium methods
– less precise than the kinetic methods
– RID and EIA systems • 5 to 1 5%
– RIA• 5 to 10%
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Assay Characteristics
• Turnaround Time – Nephelometric and turbidimetric• Kinetic methods
– Fast,within minutes• Equilibrium methods
– Up to 1 h
– RID • 24 to 48 h of incubation
– RIA • Several hours
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Electrophoresis,Laboratory Considerations
• Buffer – Barbital
• ionic strength of 0.05 • pH 8.6 • Sample is 3 to 5 µL • Support medium – 1 .5 mA per 2-cm width of cellulose acetate– 10 mA per 1-cm width of agarose medium
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• Usually five bands (albumin, α1, α2, β and y)– a sixth band • Serum is fresh • buffer containing Ca2+ ions
• Densitometry – quantification of individual bands
• Stain poorly – high proportions of lipid – Carbohydrate
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• Mask effect – Too low concentrations – over- shadowed
• Visualize bands– Amido black and Ponceau S – Coomassie brilliant blue
• Dried, record • Lipoproteins – Migrate variable • Normal control serum
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• Hyperproteinemia – Dehydration
• Inadequate water intake • Excessive water loss
– Vomiting, diarrhea, Addison’s disease, or diabetic acidosis
• Hypoproteinemia– Hemodilution
• Recumbent position – Decreases total protein concentration by 0.3 to 0.5 gIdL
• All the individual plasma proteins to the same degree• Intravenous infusions
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• Mild hyperproteinemia – Increases in APR and polyclonal immunoglobulins
• Marked hyperproteinemia – high levels of the monoclonal immunoglobulins • Multiple myeloma
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Methods (total protein)
• Biuret Method • Peptide bonds react with Cu2+ ions in alkaline solutions
to form a colored product– Presence of peptide bonds
• Tri-, oligo-, and polypeptides react– By spectrophotometry at 540 nm
– The intensity of the color produced is proportional to the number of peptide bonds
• Interference – Small peptides– Ammonium ions
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Methods Biuret Method
• Detection limit – 1 and 15 mg of protein
• Simple, sufficiently precise• A fasting serum or plasma – to decrease lipemia
• Hemolysis should be avoided
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Direct Photometric Methods
– Absorption of ultraviolet (UV) light – at 200 to 225 nm– at 270 to 290 nm
• Limitations – Uneven distribution aromatic ring – Free tyrosine and tryptophan– Uric acid– Bilirubin
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• At 200 to 225 nm– Peptide bonds are chiefly responsible for UV
absorption
• Removal of small interfering molecules– by dilution – gel filtration
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Dye-Binding Methods• CBB binds to protonated amine groups of amino
acid simple• Fast, & linear up to 150 mg/dl• Absorbance at 595 nm
• Limitation – Unequal affinities for dyes– Binding capacities of individual proteins – Inability to define a consistent material for use as a
calibrator
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• Positive interferences – Tolbutamide , high concentrations of urea
• Negative interferences – Very high concentrations of NaCl – Hydrogen chloride (HCl)
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FoIin-Ciocalteu (Lowry) Method
• Reaction with Cu2+ in alkaline solution to form copper—peptide bond protein complexes
• Folin-Ciocalteu reagent– Phosphotungstic-phosphomolybdic acid
• Tyrosine or tryptophan Reduce Cu2+ • Reduced Cu2+ form complex with Folin-Ciocalteu
reagent– Measurement at 650 - 750 nm
• Detection limit– 1 0—60 g/mL
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FoIin-Ciocalteu (Lowry) Method
• Measuring total protein in urine or CSF• Limitation– Positive interference • Drugs such as salicylates, chlorpromazine,
tetracyclines, and some sulfa drugs
– Removal of interferences • Gel filtration
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KjeldahI’s Method
• Acid digestion– Convert nitrogen in the protein to ammonium ion
• Concentration of ammonia nitrogen– Double iodides (potassium and mercuric) form a
colored complex with ammonia
• Limitation – Time consuming• Impractical for wide spread routine use
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Precipitation methods
• Precipitation of protein– Sulfosalicylic acid– Trichloroacetic acid (TCA)
• Scatter incident Light
• TCA precipitation (Another approach)
– Addition of biuret reagent to the precipitate• Suitable for a fairly large volume of specimen(urine)
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Comments• Specimen Collection and Storage– Test specimens must be– Nonhemolyzed – Cell-free
– Lipemic sera should not be assayed– Test tubes must remain covered • Dust and dirt particle contamination
– Storage conditions – Use of outdated reagents
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Calibration of Total Protein Methods
• Reference material– Bovine or human albumin• Biuret method
– Serum (or serum pool) with a normal albumin/globulin ratio• Precipitation methods• Dye-binding methods
• Calculations– Calibration curve consisting of 8 to 15 points
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