Mapa mental
Protein structure
Contenido del mapa
Protein structure
Primary
- amino acids are covalently linked together
- proteins with similar AA seqs and conformations have similar functions (i.e. DNA-binding proteins)
- point mutation in T-form hemoglobin-->sickle cell anemia
Secondary
- Alpha helix
- hydrogen bonds, which form between the carbonyl O of one amino acid and the amino H of another.
- Free rotation around these bonds
- Helical conformation allows for linear alignment of hydrogen bonds
- Maximum bond strength
- Stable conformation
- Coil of helix is clockwise or right-handed
- 3.6 residues per turn
- C═O≡H—N H bonds parallel to helical axis
- every backbone N−H group donates H bond to the backbone C=O group of AA located three or four residues earlier along the protein sequence
- R groups point outward
- Each peptide bond is trans and planar
- Disruption
- Bending of polypeptide backbone due to Pro
- Restricts rotation due to cyclic structure
- Results in absence of N—H for H-bonding in α-amino group
- electrostatic repulsion caused by proximity of like charges (i.e. Lys and Arg or Glu and Asp)
- Steric repulsion caused by proximity of bulky side chains (i.e. Val, Ile, and Thr)
- Bending of polypeptide backbone due to Pro
- Irregularities
- Found in shorter stretches than standard α-helix
- Sometimes break up regular nature of α-helix
- 310 helix: 3 residues per turn and 10 atoms in ring
- hydrogen bonds, which form between the carbonyl O of one amino acid and the amino H of another.
- Know the Ramachandran Angles!
- phi (Φ): bond between the α-carbon and amino nitrogen
- psi (Ψ): bond between α-carbon and carbonyl carbon
- Hydrogen-bonded arrangement of polypeptide chain (backbone only)
- Each amino acid residue has two bonds with free rotation
- Beta pleated sheets
- Backbone mostly extended
- Hydrogen bonds between peptide chains can be interchain or intrachain
- Polypeptide chains lie adjacent to one another
- If chains run in the same direction, the sheet will be parallel
- less stable because individual AA geometry forces H bonds to occur at an angle, making them longer and thus weaker
- If chains run in opposite direction, sheet will be antiparallel
- If chains run in the same direction, the sheet will be parallel
- H bonds perpendicular to protein chain (not parallel)
- R groups alternate above and below the plane
- Each peptide bond is trans and planar
- β-bulge
- Common nonrepetitive irregular secondary motif in antiparallel β-sheets
- Between 2 normal β-structure H bonds
- Involves 2 residues on one strand and 1 on the other
- Reverse turns
- Contain glycine
- Formed due to (steric) reasons
- Proline also encountered in reverse turns because of cyclic structure
- Alpha helix
Supersecondary
- βαβ unit (hairpin) - Two parallel β-sheets connected by α-helix
- αα unit (helix turn helix) - two antiparallel α-helices
- Motifs: Repetitive supersecondary structures
- Provide information about protein folding
- Don’t predict biological function of protein
Tertiary
- Fibrous Proteins
- Backbone of protein does not fold back on itself
- long, narrow rod
- Chains organized in parallel along single axis
- Consist of long fibers or large sheets
- mechanically strong
- H2O insoluble
- Tropocollagen
- coiled coil interaction
- triple helix
- Strands held together by H bonds involving hydroxyproline and hydroxylysine
- With age, collagen helices become cross-linked by covalent bonds formed by reactions of Lys and His residues
- Leads to tough meat in animals
- single collagen molecule
- X—Pro—Gly or X—Hydroxyproline—Gly
- Globular
- nonpolar inside, polar outside (Ion–dipole interactions with H2O environment)
- compact
- substantial sections of α-helix and β-sheet
- soluble in water and salt solutions
- Noncovalent interactions
- Backbone H bonding between polar side chains
- Hydrophobic interactions between nonpolar side chains
- Electrostatic attraction between side chains
- covalent interactions
- disulfide bridges restrict folding patterns
- Side chain metal ion coordination
- Experimental determination
- X-Ray crystallography
- Perfect crystal: all molecules have same 3-D structure and orientation
- atoms scatter X-Rays
- Fourier series analysis
- 2D NMR (aqueous solution)
- X-Ray crystallography
- Fibrous Proteins
Quaternary
- disulfides
- Allostery: Conformational change in one subunit induces change in another subunit
- van der Waals
- ionic
Denaturation
- Sodium dodecyl sulfate (SDS): disrupts hydrophobic interactions
- β-mercaptoethanol reduces disulfide bridges
- Guanidine HCl breaks H bonds
- Urea
- breaks H bonds
- Increase accessibility of RNApol disulfides to reducing agent
Hemoglobin and Myoglobin
- Myoglobin
- Structure
- single polypeptide chain of 153 amino acid residues + heme prosthetic group
- 8 α-helices,0 beta strands
- O2 binding
- Two His residues interact with heme group and O2
- Hyperbolic
- Linear at low pO2
- Curve flattens at high pO2
- All molecules bound to O2
- Function - Oxygen storage
- Requirement - Bind O2 strongly at very low pressures
- Saturation - 50% at 1 torr
- Structure
- Heme
- protoporphyrin IX
- Four 5-membered rings based on the pyrrole structure
- Linked by methine (—CH═) groups
- In hydrophobic pocket
- Fe(II) coordination
- Four N atoms of four pyrrole-type rings
- 5th coordination one of N atoms of His F8
- O2 bound at 6th coordination site
- Affinity of free heme for carbon monoxide (CO) 25,000 X >O2
- His E7 forces angled (weakened) binding
- E6V mutation in T form of Hb-->sickle cell anemia
- His E7 forces angled (weakened) binding
- protoporphyrin IX
- Hemoglobin
- Structure
- 2 alpha chains 141 residues long
- 2beta chains 146 residues long
- O2 binding
- up to 4 molecules
- Function - Oxygen transport
- Requirement - Bind strongly to O2 and release O2 easily (need 2 conformations
- p50 ≅ 26 torr (pO2 in tissues)
- 100% saturated at pO2 = 100 torr (pO2 in lungs)
- sigmoidal graph
- fetal version has gamma instead of beta chains, binds BPG less well and O2 better
- Structure
- Myoglobin
Información
- Descripción
- Mapa Mental sobre Protein structure, creado por GLORI DAS el 09/09/2018.
- Creado por
- GLORI DAS
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