Protein Estimation by Lowry’s Method

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Presentation transcript:

Protein Estimation by Lowry’s Method

Points to be covered 1)General Information about Proteins Amino acids Classification Peptide bonds 2)Importance of Lowry’s Method 3)Chemical reactions involved 4)Applications of protein estimation

1)General Information about Proteins One of the biomolecules made up of hundreds or thousands of smaller units called amino acids There are 20 different types of amino acids(Standard Amino acid) that can be combined to make a protein The sequence of amino acids determines each protein’s unique 3-dimensional structure and its specific function. The sequence of amino acid residues in a protein is defined by the sequence of a gene, which is encoded in the genetic code. Functions of proteins catalyze metabolic reactions Act as transporting molecules  Structural component

Peptide bond (amide bond) covalent chemical bond linking two consecutive amino acid monomers along synthesized when the carboxyl group of one amino acid molecule reacts with the amino group of the other amino acid molecule, causing the release of a molecule of water (Condensation reaction) A linear chain of amino acid residues linked via peptide bond is called a polypeptide

Classification of amino acids Non-Polar amino acids Glycine, Alanine, Valine, Leucine, Isoleucine, Proline, Methionine 2. Polar Amino acids Serine, Threonine, Cysteine, Asparagine, Glutamine 3. Aromatic Amino Acids Tyrosine, Tryptophan, Phenyl Alanine 4. Charged Amino Acid -vely charged Aspartate, Glutamate +vely charged Histidine, Lysine, Arginine

2)Importance of Lowry’s Method Various methods are also used Biuret Method BCA (Bicinchoninic acid assay ) Bradford Lowry’s method is widely used because of its Effective at protein concentration between 0.01-1mg/ml Sensitivity Specificity

3) Chemical reactions 1] Biuret reaction Copper reduced and electron released Alkali conditions The reaction of the cupric ions with the nitrogen atoms involved in peptide bonds leads to the displacement of the peptide hydrogen atoms under the alkaline conditions. A tri or tetra dentate chelation with the peptide nitrogen produces the "biuret" color(Blue-purple color)

Folin’s reagent is reduced to poly molybdenum (blue color) 2] Lowry’s reaction Cu+ formed during the biuret reaction reacts further with Folin’s , leading to a deeper color Folin’s reagent is reduced to poly molybdenum (blue color) Protein –Cu+ complex(Biuret complex )+ Folin’s reagent Blue color depends partly on the tyrosine and tryptophan Polymolybdenum (Deep blue)

Procedure Make Dilutions of Standard BSA(200ug/ml) viz. 50ug/ml,100ug/ml,150ug/ml,200 ug/ml Make upto 1 ml with Distilled water Simultaneously run Blank and Test(unknown) Add reagent C (freshly prepared), Wait for 10 min Add Folin’s reagent, wait for 20 min Plot a standard curve for absorbance at 740 nm against BSA concentration (μg/ml)(filter no. 4) From the standard curve obtain the concentration of unknown sample Bovine Serum Albumin (BSA) as a standard protein, because of its easy availability and  low cost with improved purity. 

4) Applications Disease diagnosis In Proteinuria: detection of peptides in urine Protein estimation of protein concentration is necessary in protein purification, electrophoresis, cell biology, molecular biology, and other research applications.