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Dye Binding of Serum Albumin Study of importance of interactions between biomolecules Molecules with complementary surfaces interact.

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Presentation on theme: "Dye Binding of Serum Albumin Study of importance of interactions between biomolecules Molecules with complementary surfaces interact."— Presentation transcript:

1 Dye Binding of Serum Albumin Study of importance of interactions between biomolecules Molecules with complementary surfaces interact

2 Dye Binding of Serum Albumin Study of importance of interactions between biomolecules Molecules with complementary surfaces make a “good fit” (“induced fit” “lock and key”) a b c Substrate + Enzyme a b c ES complex a b c

3 Dye Binding of Serum Albumin Molecules with complementary surfaces make a “good fit” Antibody-antigen

4 Dye Binding of Serum Albumin Molecules with complementary surfaces make a “good fit” Antibody-antigen

5 Dye Binding of Serum Albumin Serum albumin - protein used to transport nonsoluble molecules through the bloodstream Carries: bilirubin, fatty acids, hormones, dyes bilirubin Bromphenol blue (phenol red w/o Br) Fatty acids

6 Dye Binding of Serum Albumin Investigate specificity of protein for small dyes, bromphenol blue and phenol red Determine whether NATIVE STRUCTURE of protein is required to bind dyes

7 Dye Binding of Serum Albumin NATIVE STRUCTURE of protein vs. denatured Denaturation affects weak interactions, such as H-bonds Denature proteins by: Heat, extreme pH, add organics (alcohol, acetone) Add urea, guanidine hydrochloride, detergent (SDS) Add reducing agent to break S-S (  -ME, DTT) Renaturation = regaining native structure and biological activity Renature proteins by: refolding protein ( remake H-bonds, S-S, etc )

8 Dye Binding of Serum Albumin NATIVE STRUCTURE of protein vs. denatured Relatively strong, covalent disulfide bond Relatively weak (e.g, H ) bonds SS S S

9 Dye Binding of Serum Albumin NATIVE STRUCTURE of protein vs. denatured Increased thermal energy “disrupts” relatively weak bonds (ionic, H bonds) S-S SS Heated @ 95 o C for 4 min

10 Dye Binding of Serum Albumin NATIVE STRUCTURE of protein vs. denatured  mercaptoethanol (DTT): Disrupts any covalent, disulfide bonds between cysteine amino acids S-S  ME 

11 Dye Binding of Serum Albumin NATIVE STRUCTURE of protein vs. denatured SDS is an amphipathic molecule with a strong negative charge + polypeptide

12 Dye Binding of Serum Albumin Determine molecular weight of serum albumin Study binding specificity of protein for dyes using column Determine effects of SDS on protein-dye interactions Two samples: +SDS-SDS Serum albumin Bromphenol blue Phenol red SDS 1. Load -SDS sample onto your column and separate measuring Ve for colored dyes (BPB and PR) 2. Load +SDS sample onto your column and separate measuring Ve for colored dyes (BPB and PR)

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