Date post: | 13-Jan-2017 |
Category: |
Science |
Upload: | wilhelmina-annie-mensah |
View: | 389 times |
Download: | 2 times |
Proteins
Wilhelmina Annie MensahDept. Of Med. Bchem.
UGMS , Ghana 105/01/23
Amino acids are the basic unit of proteins
Amino acids consist of C, H, O and N (S & P)
Proteins have a 3 dimensional globular shape
Proteins
• Peptide bonds connect amino acids to form polypeptide chains
• One or more polypeptide chains make up a protein
Proteins Structure
305/01/23
levels of Proteins Structure
405/01/23
Functions of Proteins 1. Transport of substances in the body .
E.g. Haemoglobin transports oxygen.
505/01/23
Functions of Proteins 2.Enzymes which catalyze chemical reactions in the
body are proteins
Substrate (lactose) Glucose Galactose
605/01/23
Functions of Proteins 3.Defence function .e.g Immunoglobulins(antibodies)
705/01/23
Functions of Proteins 4.In gene expression: Histones are the proteins which the DNA double helix is wrapped around
805/01/23
6. Nutrient and storage .E.g albumen of egg, Ferritin that stores iron.
Functions of Proteins
7.Proteins are infective agents.e.g Prions which cause mad cow disease are proteins
905/01/23
8.Some toxins are proteins E.g Enterotoxin of cholera microorganism.
9.Some proteins provide structural strength and elasticity to the organs and vascular system. E.g Collagen and elastin of bone matrix and ligaments.
10. Some proteins are components of structures of tissues. E.g α-keratin is present in hair and epidermis
Functions of Proteins
1005/01/23
Nucleic Acids
1105/01/23
• They are made up of C, H, N, O, P
• The basic unit is a nucleotide
(nucleoside)
Nucleic Acids
1205/01/23
Sugar
Base
= Sugar + Base= Sugar + Base
1305/01/23
Sugar
Base
Phosphate
NucleosideNucleoside
1405/01/23
Glycosidic Bond is a bond between a sugar and another group
Ester Bond
Glycosidic Bond
Ester Bond is C-O-R and the oxygen is bounded to something else 1505/01/23
Composition of Nucleotides
Sugar
Bases
Phosphate
1605/01/23
Composition of Nucleotides
• Pentoses (5-C sugars or carbohydrate)• Numbering of sugars is “primed”
1705/01/23
Sugars
Ribose : forming Ribonucelotides
Deoxyribose: forming Deoxynucelotides (d-Nucleotides)
Oxygen missing
1805/01/23
Sugar (types)
fused five- and six-membered rings
Pyrimidines – N 1 forms glycosidic bond with sugarPurines -N 9 forms glycosidic bond with the sugar
six membered rings
1905/01/23
Bases
Adenine A
Guanine G
Thymine T Uracil U
Cytosine C2005/01/23
Bases
2105/01/23
Bases
2205/01/23
Bases
Bases Occurrence Bases Occurrence
Ribonucleotides only
Ribonucleotides & D-nucleotides
D-nucloetides only
2305/01/23
• Phosphates can be bonded to either C5 or C3Phosphate GroupsPhosphate Groups
Ester Bond
•They are linked by an Ester bond
2405/01/23
Mono, Di, Tri phosphate GroupsMono, Di, Tri phosphate Groups
Nucleoside 5’-Monophosphate
Nucleoside 5’- Diphosphate
Nucleoside 5’- Triphosphate
2505/01/23
• Purine nucleosides end in “-sine” “-sine” – Ribonucleoside Deoxynucleoside
• Adenosine Deoxyadenosine• Guanosine Deoxyguanosine
Naming Conventions of NucleosidesNaming Conventions of Nucleosides
Pyrimidine nucleosides end in “-dine”“-dine”– Ribonucleoside Deoxynucleoside
• Deoxythymidine • Cytidine Deoxycytidine• Uridine 2605/01/23
Start with the nucleoside name from above and add “mono-”, “di-”, or “triphosphate”
Naming Conventions of NucleotidesNaming Conventions of Nucleotides
RibonucleotidesRibonucleotides
PurinesPurinesAdenosine monophosphate(AMP), ADP, ATPGuanosine monophosphate(GMP), GDP, GTP
PyrimindinesPyrimindinesCytidine Monophosphate, CDP, CTPUridine Monophosphate, UDP, UTP
2705/01/23
Naming Conventions of NucleotidesNaming Conventions of Nucleotides
DeoxynucleotidesDeoxynucleotides
PurinesPurinesDeoxyadenosine monophosphate (d-AMP), d-ADP, d-ATPd- Guanosine Monophosphate, d-GDP, d-GTP
PyrimindinesPyrimindinesd- Cytidine Monophosphate, d-CDP, d-CTPd- thymidine Monophosphate, d-TDP, d-TPP
2805/01/23
Nucleotides are joined together by Phosphodiester bonds
ester bondester bond
ester bondester bond
Phosphodiester bondPhosphodiester bond
2905/01/23
Phosphodiester Bond (linkages)
Voet, Voet & Pratt 2013 Fig 3.3a,b
Nucleic Acids : Polymers of nucleotidesNucleic Acids : Polymers of nucleotides
Nucleic acid with deoxy ribose sugars---Deoxyribonucleic acid (DNA)
Nucleic acid with Contains ribose sugar---Ribonucleic acid(RNA)
3005/01/23
Bases in Nucleic Acids
3105/01/23
Memory Check
3205/01/23
Double helix ( 2 polynucleotide chains wound into the double helix) Base pairing between chains with H bonds
In base pairing A – T (double bond) C – G (triple bond)
Nucleic Acids : DNANucleic Acids : DNA
3305/01/23
Single stranded
It is made from the DNA template molecule
Uracil replaces the base thymine
During base pairing U----A
Nucleic Acids : RNANucleic Acids : RNA
3405/01/23
1. They are involved in the storage of genetic information.
Functions of nucleic acid in the cell
3505/01/23
1. They are involved in the expression of genetic information.
Functions of nucleic acid in the cell
3605/01/23
Functions of nucleic acid in the cell
1. They are involved in the transfer of genetic information.
3705/01/23
Some nucleic acids acts as enzymes and coenzymes. E.g. RNA (ribozyme) is coenzyme for telomerase which seals ends of chromosomes.
Functions of nucleic acid in the cell
3805/01/23
Nucleoside Derivatives and their functions
Adenosine derivatives
Guanosine derivative
Cytidine derivatives
Uridine derivatives
3905/01/23
Adenosine Triphosphate (ATP)
3'-5'-Cyclic Adenosine Monophosphate, “(cAMP or cyclic AMP)
Flavin Adenine Dinucleotide (FAD & FMN)
Nicotinaminde Adenine Dinucleotide (NAD+ & NADP)
S-adenosylmethionine (SAM)
Common Adenosine Derivatives
4005/01/23
ATP StructureATP Structure
4105/01/23
Adenosine Derivatives
1. Energy storage and transfer
4205/01/23
Cyclic AMP StructureCyclic AMP Structure
4305/01/23
Adenosine Derivatives
1. Second messenger in signal transduction
2.Regulate metabolism e.g. glycogen breakdown, lipids breakdown etc
4405/01/23
Flavin Adenine Dinucleotide (FAD(HFlavin Adenine Dinucleotide (FAD(H22)) & FMN(H & FMN(H22) Structure) Structure
Flavin Mononucloetide
(FMN)
Flavin
Coenzyme functioning as carrier of hydrogen and electrons in some redox reactions
sugar
+ H2
Riboflavin(Vit B 2)
FAD
FMN(HFMN(H22) or FAD(H) or FAD(H22))
phosphate
4505/01/23
Nicotinamide Adenine DinucleotideNicotinamide Adenine DinucleotideNAD (H)NAD (H)++ and NADP(H) and NADP(H)++ Structures Structures
+ H
Coenzyme functioning as carrier of hydrogen
and electrons some redox reactions
NADP
NADPH
NAD
4605/01/23
Coenzyme A StructureCoenzyme A Structure
Coenzyme serving as acyl group – R(CO) carrier in certain enzymatic reactions
4705/01/23
S- adenosylmethionine StructureS- adenosylmethionine Structure
Methyl (CH3) donor in methylation reactions4805/01/23
S-adenosylmethionine (SAM)
Common Adenosine Derivatives
4905/01/23
Guanosine Derivative
1. Energy store
2.Energy source for Protein synthesis and Gluconeogenesis
5005/01/23
Uracil Derivatives
5105/01/23
Cytidine Derivatives
CMP-N acetylneuraminic acid (CMP-NANA) required for the biosynthesis of glycoproteins
CDP-choline- required for the biosynthesis of sphingolipids (component of cell membrane of brain and nervious tissues).
CTP- required for the biosynthesis of phosphoglycerides (component of cell membrane)
sphingosine
5205/01/23
Synthetic Analogues of Nucleotides
5305/01/23
Synthetic Analogues of Nucleotides:Anti-tumour agents used in chemotherapy
Interfere with the synthesis of DNA and thereby preferentially kill rapidly dividing cells such as tumor cells.
5405/01/23
Synthetic Analogues of Nucleotides:Anti-tumour agents used in chemotherapy
5505/01/23
Synthetic Analogues of Nucleotides:Anti-Viral agents
Used to interfere with the replication of viruses by terminating DNA synthesis
5605/01/23
Synthetic Analogues of Nucleotides:Treatment of Gout
Caused by accumulation of uric acid
5705/01/23
Precursors of nucleic acids, DNA & RNA
Components of important co-enzymes ( like NAD+ and FAD, Co-enzyme A)
Storage and transfer of energy (ATP and GTP )
Storage and transfer of genetic information (DNA & RNA)
5805/01/23
Biomedical importance of nucleotides
5905/01/23
Biomedical importance of nucleotides
Memory Check
6005/01/23
Memory CheckMemory Check
Ribonucleotides only
Ribonucleotides & D-nucleotides
D-nucloetides only
6105/01/23
S-adenosylmethionine (SAM)
Memory CheckMemory Check
6205/01/23
Memory CheckMemory Check
6305/01/23
Memory CheckMemory Check
6405/01/23
Memory CheckMemory Check
6505/01/23
Memory CheckMemory Check
6605/01/23
Memory CheckMemory Check
6705/01/23
Memory CheckMemory Check
6805/01/23
6905/01/23
Memory Check
7005/01/23
Memory CheckMemory Check
7105/01/23
Memory CheckMemory Check
7205/01/23
Memory checkMemory check
7305/01/23
7405/01/23
Nucleotide ChemistryNucleotide ChemistryBAHS 233BAHS 233
Thank you7505/01/23
Minor Pyrimidine nucleosides
7605/01/23
Minor Purine Nucleosides
7705/01/23