1. Proteins account for more than 50% of the dry mass of most cells
Concept 5.4: Proteins have many structures, resulting in a wide range of functions
Proteins account for more than 50% of the dry mass of most cells
Protein functions include structural support, storage, transport, cellular communications, movement, and defense against foreign substances
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2. Table 5-1
Table 5-1

3. Enzymes are a type of protein that acts as a catalyst to speed up chemical reactions
Enzymes can perform their functions repeatedly, functioning as workhorses that carry out the processes of life
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4. Substrate (sucrose) Glucose Enzyme (sucrase) OH H2O Fructose H O
Fig. 5-16
Substrate
(sucrose)
Glucose
Enzyme
(sucrase) OH
H2O
Fructose
Figure 5.16 The catalytic cycle of an enzyme H O

5. Polypeptides are polymers built from the same set of 20 amino acids
A protein consists of one or more polypeptides
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6. Amino acids are organic molecules with carboxyl and amino groups
Amino Acid Monomers
Amino acids are organic molecules with carboxyl and amino groups
Amino acids differ in their properties due to differing side chains, called R groups
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7. Fig. 5-UN1
 carbon
Amino
group
Carboxyl
group

8. Figure 5.17 The 20 amino acids of proteins
Nonpolar
Glycine
(Gly or G)
Alanine
(Ala or A)
Valine
(Val or V)
Leucine
(Leu or L)
Isoleucine
(Ile or I)
Methionine
(Met or M)
Phenylalanine
(Phe or F)
Trypotphan
(Trp or W)
Proline
(Pro or P)
Polar
Serine
(Ser or S)
Threonine
(Thr or T)
Cysteine
(Cys or C)
Tyrosine
(Tyr or Y)
Asparagine
(Asn or N)
Glutamine
(Gln or Q)
Figure 5.17 The 20 amino acids of proteins
Electrically
charged
Acidic
Basic
Aspartic acid
(Asp or D)
Glutamic acid
(Glu or E)
Lysine
(Lys or K)
Arginine
(Arg or R)
Histidine
(His or H)

9. Amino acids are linked by peptide bonds
Amino Acid Polymers
Amino acids are linked by peptide bonds
A polypeptide is a polymer of amino acids
Polypeptides range in length from a few to more than a thousand monomers
Each polypeptide has a unique linear sequence of amino acids
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10. Amino end (N-terminus) Carboxyl end (C-terminus)
Fig. 5-18
Peptide
bond
(a)
Side chains
Peptide
bond
Figure 5.18 Making a polypeptide chain
Backbone
Amino end
(N-terminus)
Carboxyl end
(C-terminus)
(b)

11. Protein Structure and Function
A functional protein consists of one or more polypeptides twisted, folded, and coiled into a unique shape
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12. A ribbon model of lysozyme A space-filling model of lysozyme
Fig. 5-19
Groove
Groove
Figure 5.19 Structure of a protein, the enzyme lysozyme
(a)
A ribbon model of lysozyme
(b)
A space-filling model of lysozyme

13. A protein’s structure determines its function
The sequence of amino acids determines a protein’s three-dimensional structure
A protein’s structure determines its function
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14. Antibody protein Protein from flu virus
Fig. 5-20
Antibody protein
Protein from flu virus
Figure 5.20 An antibody binding to a protein from a flu virus

15. Four Levels of Protein Structure
The primary structure of a protein is its unique sequence of amino acids
Secondary structure, found in most proteins, consists of coils and folds in the polypeptide chain
Tertiary structure is determined by interactions among various side chains (R groups)
Quaternary structure results when a protein consists of multiple polypeptide chains
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16. Primary structure is determined by inherited genetic information
Primary structure, the sequence of amino acids in a protein, is like the order of letters in a long word
Primary structure is determined by inherited genetic information
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

17. +H3N Primary Structure Amino end Amino acid subunits 1 5 10 15 20 25
Fig. 5-21a
Primary Structure 1 5
+H3N
Amino end 10
Amino acid
subunits 15
Figure 5.21 Levels of protein structure—primary structure 20 25

18. The coils and folds of secondary structure result from hydrogen bonds between repeating constituents of the polypeptide backbone
Typical secondary structures are a coil called an  helix and a folded structure called a  pleated sheet
For the Cell Biology Video An Idealized Alpha Helix: No Sidechains, go to Animation and Video Files.
For the Cell Biology Video An Idealized Alpha Helix, go to Animation and Video Files.
For the Cell Biology Video An Idealized Beta Pleated Sheet Cartoon, go to Animation and Video Files.
For the Cell Biology Video An Idealized Beta Pleated Sheet, go to Animation and Video Files.
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19. Secondary Structure  pleated sheet Examples of amino acid subunits
Fig. 5-21c
Secondary Structure
 pleated sheet
Examples of
amino acid
subunits
Figure 5.21 Levels of protein structure—secondary structure
 helix

20. Tertiary structure is determined by interactions between R groups, rather than interactions between backbone constituents
These interactions between R groups include hydrogen bonds, ionic bonds, hydrophobic interactions, and van der Waals interactions
Strong covalent bonds called disulfide bridges may reinforce the protein’s structure
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21. Hydrophobic interactions and van der Waals interactions Polypeptide
Fig. 5-21f
Hydrophobic
interactions and
van der Waals
interactions
Polypeptide
backbone
Hydrogen
bond
Disulfide bridge
Figure 5.21 Levels of protein structure—tertiary and quaternary structures
Ionic bond

22. Quaternary structure results when two or more polypeptide chains form one macromolecule
Collagen is a fibrous protein consisting of three polypeptides coiled like a rope
Hemoglobin is a globular protein consisting of four polypeptides: two alpha and two beta chains
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23. Polypeptide  Chains chain Iron Heme  Chains Hemoglobin Collagen
Fig. 5-21g
Polypeptide
chain
 Chains
Iron
Figure 5.21 Levels of protein structure—tertiary and quaternary structures
Heme
 Chains
Hemoglobin
Collagen

24. Sickle-Cell Disease: A Change in Primary Structure
A slight change in primary structure can affect a protein’s structure and ability to function
Sickle-cell disease, an inherited blood disorder, results from a single amino acid substitution in the protein hemoglobin
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25. Fig. 5-22
Normal hemoglobin
Sickle-cell hemoglobin
Primary
structure
Primary
structure
Val
His
Leu
Thr
Pro
Glu
Glu
Val
His
Leu
Thr
Pro
Val
Glu 1 2 3 4 5 6 7 1 2 3 4 5 6 7
Exposed
hydrophobic
region
Secondary
and tertiary
structures
Secondary
and tertiary
structures
 subunit
 subunit    
Quaternary
structure
Normal
hemoglobin
(top view)
Quaternary
structure
Sickle-cell
hemoglobin    
Function
Molecules do
not associate
with one
another; each
carries oxygen.
Function
Molecules
interact with
one another and
crystallize into
a fiber; capacity
to carry oxygen
is greatly reduced.
Figure 5.22 A single amino acid substitution in a protein causes sickle-cell disease
10 µm
10 µm
Red blood
cell shape
Normal red blood
cells are full of
individual
hemoglobin
moledules, each
carrying oxygen.
Red blood
cell shape
Fibers of abnormal
hemoglobin deform
red blood cell into
sickle shape.

26. What Determines Protein Structure?
In addition to primary structure, physical and chemical conditions can affect structure
Alterations in pH, salt concentration, temperature, or other environmental factors can cause a protein to unravel
This loss of a protein’s native structure is called denaturation
A denatured protein is biologically inactive
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27. Denaturation Normal protein Denatured protein Renaturation Fig. 5-23
Figure 5.23 Denaturation and renaturation of a protein
Normal protein
Denatured protein
Renaturation

28. What type of bond joins two amino acids?
Protein Questions
What type of bond joins two amino acids?
Peptide, covalent
Name the 2 common secondary structures of a protein.
 helix and  pleated sheet
List the possible types of interactions at the tertiary level of a protein.
Hydrophobic / Hydrophillic, Van der Waals, Hydrogen bonding, Disulfide bridge, ionic bonding

29. Concept 5.5: Nucleic acids store and transmit hereditary information
The amino acid sequence of a polypeptide is programmed by a unit of inheritance called a gene
Genes are made of DNA, a nucleic acid
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30. The Roles of Nucleic Acids
There are two types of nucleic acids:
Deoxyribonucleic acid (DNA)
Ribonucleic acid (RNA)
DNA provides directions for its own replication
DNA directs synthesis of messenger RNA (mRNA) and, through mRNA, controls protein synthesis
Protein synthesis occurs in ribosomes
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31. DNA 1 Synthesis of mRNA in the nucleus mRNA NUCLEUS CYTOPLASM mRNA 2
Fig
DNA 1
Synthesis of
mRNA in the
nucleus
mRNA
NUCLEUS
CYTOPLASM
mRNA 2
Movement of
mRNA into cytoplasm
via nuclear pore
Ribosome
Figure 5.26 DNA → RNA → protein 3
Synthesis
of protein
Amino
acids
Polypeptide

32. The Structure of Nucleic Acids
Nucleic acids are polymers called polynucleotides
Each polynucleotide is made of monomers called nucleotides
Each nucleotide consists of a nitrogenous base, a pentose sugar, and a phosphate group
The portion of a nucleotide without the phosphate group is called a nucleoside
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33. (a) Polynucleotide, or nucleic acid (c) Nucleoside components: sugars
Fig. 5-27
5 end
Nitrogenous bases
Pyrimidines
5C
3C
Nucleoside
Nitrogenous
base
Cytosine (C)
Thymine (T, in DNA)
Uracil (U, in RNA)
Purines
Phosphate
group
Sugar
(pentose)
5C
Adenine (A)
Guanine (G)
3C
(b) Nucleotide
Sugars
3 end
Figure 5.27 Components of nucleic acids
(a) Polynucleotide, or nucleic acid
Deoxyribose (in DNA)
Ribose (in RNA)
(c) Nucleoside components: sugars

34. Nucleoside = nitrogenous base + sugar
Nucleotide Monomers
Nucleoside = nitrogenous base + sugar
There are two families of nitrogenous bases:
Pyrimidines (cytosine, thymine, and uracil) have a single six-membered ring
Purines (adenine and guanine) have a six-membered ring fused to a five-membered ring
In DNA, the sugar is deoxyribose; in RNA, the sugar is ribose
Nucleotide = nucleoside + phosphate group
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35. Nucleotide Polymers
Nucleotide polymers are linked together to build a polynucleotide
Adjacent nucleotides are joined by covalent bonds that form between the –OH group on the 3 carbon of one nucleotide and the phosphate on the 5 carbon on the next
These links create a backbone of sugar-phosphate units with nitrogenous bases as appendages
The sequence of bases along a DNA or mRNA polymer is unique for each gene
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36. The DNA Double Helix
A DNA molecule has two polynucleotides spiraling around an imaginary axis, forming a double helix
In the DNA double helix, the two backbones run in opposite 5 → 3 directions from each other, an arrangement referred to as antiparallel
One DNA molecule includes many genes
The nitrogenous bases in DNA pair up and form hydrogen bonds: adenine (A) always with thymine (T), and guanine (G) always with cytosine (C)
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37. 5' end 3' end Sugar-phosphate backbones Base pair (joined by
Fig. 5-28
5' end
3' end
Sugar-phosphate
backbones
Base pair (joined by
hydrogen bonding)
Old strands
Nucleotide
about to be
added to a
new strand
3' end
Figure 5.28 The DNA double helix and its replication
5' end
New
strands
5' end
3' end
5' end
3' end

38. Nucleic Acid Questions
What are the “parts” of a nucleotide?
Sugar, phosphate and nitrogen base
Name the purines and pyrimidines.
Purine – adenine and guanine
Pyrimidine – thymine, cytosine and uracil
What two molecules make up the uprights of DNA?
Nitrogen bases held together by hydrogen bonds