Amino acids, Proteins and DNA revision mindmap
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- Created on: 23-01-19 19:08
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- Amino acids, Proteins and DNA
- Amino Acids
- Structure
- Amine group - NH2
- Protonated by acids
- Acylation with acyl chlorides
- Nucleophilic substitution with haloalkanes
- Variable side chain
- Carboxylic Acid group - COOH
- Deprotonated by bases
- Esterification with alcohols
- Amine group - NH2
- Naming
- [carbon with amine group] - AMINO_____ANOIC ACID
- Number from the end with the COOH group
- [carbon with amine group] - AMINO_____ANOIC ACID
- Acid-Base properties
- High pH
- Anion COO-
- Low pH
- Cation NH3+
- Isoelectric pH
- Zwitterion NH3+ and COO-
- Zwitterions also exist in the crystalline form of the amino acid
- Both positive and negative parts, so ionic bonding occurs
- Zwitterions also exist in the crystalline form of the amino acid
- Zwitterion NH3+ and COO-
- High pH
- Reactions
- Nucleophilic Addition - Elimination
- Warm an amino acid gently with acyl chloride
- Forms an N-substituted amide
- Warm an amino acid gently with acyl chloride
- Esterification
- Heat amino acid with ethanol and a few drops conc. H2SO4
- Nucleophilic Addition - Elimination
- Structure
- Proteins
- Structure
- Primary
- String of amino acids held together by peptide bonds
- Secondary
- Primary structure folds
- Alpha helix
- Held together by hydrogen bonds between C=O and N-H groups
- Beta pleated
- Held together by hydrogen bonds between C=O and N-H groups
- Beta pleated
- Tertiary
- 3D structure
- ionic attractions, hydrogen bonding and Van der Waal's forces
- If cysteine amino acids are present, disulphide bridges form
- Primary
- Formation
- Condensation reaction between amino acids
- Forms a peptide bond O=C-N-H
- Hydrolysis
- Uses enzymes or strong acid to break the peptide bond
- Secondary and tertiary structures rapidly broken down and the chain unravels
- Amino acids formed by protein hydrolysis can be identified by TLC
- Condensation reaction between amino acids
- Enzymes
- Biological catalyst
- Large molecules
- Mr above 10,000
- Bind at active sites
- Highly stereospecific so only one enantiomer catalyses the reaction
- Inhibitors
- Untitled
- Structure
- DNA
- Structure
- 2-deoxyribose sugar
- Joined by condensation reaction at Carbon 5
- Phosphate group PO4H3
- Joined by condensation reaction at Carbon 1
- One of 4 bases Adenine, Cytosine, Guanine, Thymine
- Joined by condensation reaction at Carbon 1
- Phosphate group PO4H3
- Joined by condensation reaction at Carbon 5
- Phosphate group PO4H3
- Joined by condensation reaction at Carbon 1
- One of 4 bases Adenine, Cytosine, Guanine, Thymine
- Joined by condensation reaction at Carbon 1
- Double helix shape formed by hydrogen bonding between bases
- 2 H-bonds between A and T
- 3 H-bonds between C and G
- 2-deoxyribose sugar
- Anticancer drugs
- Cisplatin
- Effective drug against testicular cancer
- Square planar transition metal complex containing Platinum
- Forms coordinate bonds with guanine molecules (Ligand replacement reaction)
- Guanine molecules on same strand
- Distorts DNA shape, preventing replication
- Guanine molecules on same strand
- Also affects healthy cells that replicate frequently
- Give low doses
- Target only tumour cells
- Reduces adverse effects
- Give low doses
- Reduces adverse effects
- Isomer, transplatin, has no significant anticancer properties
- Target cells that divide rapidly
- Cisplatin
- Structure
- Amino Acids
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