Protein Synthesis:

 

Prokaryotes Introduction:

 

The genetic material is a double stranded or it can be single stranded polynucleotide chain with a polarity and with a specific sequence with polarity.   The mRNA is another polynucleotide chain with a specific sequence with a polarity.  Protein is a polypeptide chain of amino acids with sequence specificity and it has a polarity.  All of them exhibit linearity, where the information flow is from DNA to RNA and RNA to protein, all are linear chains, which is the basis for Crick’s Central Dogma.  Francis Crick proposed this par excellent dogma before the discovery of Reverse Transcriptase by Baltimore and Timmins.   But the revised Central Dogma, forced to revise the central dogma, on the basis of findings that RNA can be transcribed into DNA, so DNA to RNA and RNA to DNA is now an accepted fact, however RNA to protein is the final step in flow of information.

 

                                  Codon Directory:

 

 

U

 

C

 

A

 

G

 

 

U

UUU

UUCphe

UUA

UUGleu

F

F

L

L

UCU

UCC

UCA

UCGser

S

S

S

S

UAU

UACtyr

UAAstop

UAGstop

Y

Y

-

-

UGU

UGCcys

UGAstop

UGGtrp

C

C

-

W

U

C

A

G

C

CUU

CUC

CUA

CUGleu

L

L

L

L

CCU

CCC

CCA

CCGpro

P

P

P

P

CAU

CAChis

CAA

CAGgln

H

H

Q

Q

CGU

CGC

CGA

CGGarg

R

R

R

R

U

C

A

G

 

A

AUU

AUC

AUAile

AUGmet

I

I

I

M

ACU

ACC

ACA

ACGthr

T

T

T

T

 

AAU

AACasn

AAA

AAGlys

N

N

K

K

AGU

AGCser

AGA

AGGarg

S

S

R

R

U

C

A

G

G

GUU

GUC

GUA

GUGval

V

V

V

V

GCU

GCC

GCA

GCGala

A

A

A

A

GAU

GACasp

GAA

GAGglu

D

D

E

E

GGU

GGC

GGA

GGGgly

G

G

G

G

U

C

A

G

 

 

 

 

                                  Anti Codon Directory ?:

                                 

 

A

 

G

 

U

 

C

 

 

 

AAA

AAGphe

AAU

AACleu

 

AGA

AGG

AGU

AGCser

 

AUA

AUGtyr

-

-

 

ACA

ACGcys

-

ACCtrp

 

A

G

U

C

G

GAA

GAG

GAU

GACleu

 

GGA

GGG

GGU

GGCpro

 

GUA

GUGhis

GUU

GUCgln

 

GCA

GCG

GCU

GCCarg

 

A

G

U

C

U

UAA

UAG

UAUilu

UACmet

 

UGA

UGG

UGU

UGCthr

 

UUA

UUGasn

UUU

UUClys

 

UCA

UCGser

UCU

UCCarg

 

A

G

U

C

C

CAA

CAG

CAU

CACval

 

CGA

CGG

CGU

CGCval

 

CUA

CUGasp

CUU

CUCglu

 

CCA

CCG

CCU

CCCgly

 

A

G

U

C

           

Expected anticodon sequences but one does not find all the expected anticodons in tRNAs, but tRNAs with isoforms decode all the 63 codons; no anticodons for Terminator codons.

 

 

Amino acid basic structure

 

Amino acid specificity.  Acronyms

 

Alanine A

Leucine L

Arginine R

Lysine K

Asparagine N

Methionine M

Aspartate D

PhenylalanineF

Cysteine C

Proline P

Glutamate E

Serine S

Glutamine Q

 

Glycine G

ThreonineT

Histidine H

Tryptophane W

Isoleucine I

Tyrosine Y

Leucine L

Valine V

 

 

 

http://employees.csbsju.edu/

 

Each amino acid contains an "amine" group (NH3) and a "carboxy" group (COOH) (shown in black in the diagram).The amino acids vary in their side chains (indicated in blue in the diagram).The eight amino acids in the orange area are nonpolar and hydrophobic. The other amino acids are polar and hydrophilic ("water loving"). The two amino acids in the magenta box are acidic ("carboxy" group in the side chain).

The three amino acids in the light blue box are basic ("amine" group in the side chain).

 

 

Glycolytic and Krebs’s cycle reactions are used in generating most of the amino acids. https://www.boundless.com

 

The genetic code

 

Degeneracy of the genetic code

To encode 20 (21) amino acids, combination of two nucleotides is not enough (4X4=16). Three nucleotides are too many (4x4x4=64), 44 excess. This excess number is compensated for having isoforms of tRNA and degenerate codons where the last nucleotide wobbles.  The same amino acid can be recognized by more than one codon and the same codon can be recognized by more than one of the isoform of anticodon. Room for innovation- Moreover, amino acids with similar properties can be substituted for each other without changing the structure and function of a protein.

 

• Six possible translation frames for every nucleotide stretch

– GCU.UGU.UUA.CGA.AUU.A 􀃆 -Ala – Cys Leu Arg Ile -

– G.CUU.GUU.UAC.GAA.UUA 􀃆 - Leu Val Tyr Glu Leu

 

Most of the tRNAs carry three anticodons, but the anticodons need not  be the same number as of codons; they have evolved what we call as wobble mechanism, where the last nucleotide in tRNA that is from 5’end can base pair with different degenerate nucleotides found in mRNA codons. There are no tRNAs that can decode terminator codons.

 

 

Diagram showing the various modified nucleotides of tRNAs that are found in the wobble position in the anticodon. The top half shows the wobble nucleotides of the anticodon in blue and the various nucleotides (in red) of the wobble position of the codon that can be found in non-Watson-Crick base-pairs. The lower panel illustrates the opposite showing the wobble nucleotides of the codon in blue and the associated wobble nucleotides of the anticodon in red; http://themedicalbiochemistrypage.org/

 

Revised wobble base pairing;

 

tRNA5’ anticodon

mRNA 3’codon

G

U, C

C

G

 

K2C

A

A

U, C (A), G

U unmodified

U, C,’ A’, G

Xm^5S@,Xm^5Um,

Um,Xm^5U

 

A, (G)

Xo^5U

U, A ,G

I

A, A, G

 

 

 

Revised codon and anticodon showing tRNA 5’nucleotide can base pair with more than one non complementary last nucleotide of the codon.

 

tRNAs and Anticodon Wobble;;http://www.sci.sdsu.edu/

 

Wobble; https://www.mun.ca/biology

 

 

 

 

 

 

There are 3 stop codons for every 64 combination of triplet nucleotides; long ORFs are unlikely; probably genes in some viruses contain as many as four overlapping frames and they are functional.

 

 

In bacterial systems, transcription and translation events are coupled and in eukaryotes the events are uncoupled.   Bacterial cells don’t have intracellular compartmentation.   In eukaryotes cytoplasm is compartmentalized where a large number of the ribosomes translate in free-state and equal numbers of proteins, which are secretary and membrane components, are translated on endoplasmic membranes.    In bacteria, coupled transcription and translation has advantages, for the 5’end, as bound by ribosomes, is protected from exonuclease activity.   In EK cells, RNAs are transcribed and processed in the nucleus, and then transported into the cytoplasm.  In cytoplasm ribosomes engage mRNAs in protein synthesis at different loci, one at the so-called Free State and another bound on endoplasmic reticulum.   These are designed to the needs of cells, where certain proteins are secreted out or destined to plasma membranes and endoplasmic reticulum and other cellular milieu.  Many proteins are destined to different cell organelles and intracellular structures.    Localization of protein synthesis is of a significant feature.

 

This simple diagram shows the bacterial transcription and translation goes hand in hand; this coupled process is absolutely required for the 5’ end of the emerging mRNA has no protection from 5’exonucleases. http://nitro.biosci.arizona.edu/ and http://www.bio.utexas.edu/

 

The rate of protein synthesis varies, from 15 to 20 amino acids per second.   A single mRNA can be associated with more than one ribosome, ten to thirty or more; this depends on the length of mRNA. Polysome formation further enhances the rate of protein synthesis.   How ribosomes, molecular machines accelerate or decelerate the rate of synthesis is not very clear.

 

Process of translation goes through in stepwise but progressive mode.   Chain initiation, chain elongation and chain termination are three important steps and each step can be regulated.  Translation is also regulated.

 

 

Factors and Other Components Required for Protein Synthesis:

 

Events

Factor

Mol.wt (KD)

Number per cell

Function

Chain Initiation

 

 

 

 

 

IF-1

8.1(7.8)

1 per7 ribosomes

Assists IF3

 

IF-2

97.9 (97.9)

1 per/7 ribosomes

Bind to i tRNA

 

IF-3

20.7 (19.8)

1 per 7 ribosomes

aids 30S dissociation , binds mRNA

Chain elongation

 

 

 

 

 

EF-Tu

43.225

10:1(~100,000)

binds to a.a tRNA

 

EF-Ts

31.0

1:1 (~10000)

GEF

 

EF-G

77.444

1:1 (~20000)

translocation

Chain Termination

-

 

 

 

 

RF-1

39.6 UAA,UAG

1 per 20 ribs

Release protein chain

 

RF-2

UAA.UGA

1 per 20 ribs

 

 

RF-3

58

 

Release of RF1 and 2

 

RRF

20.3 (~184a.a)

 

Ribosome recycling factor

Initiator tRNAs

~6000 per cell

 

 

 

Amino acyl tRNAs

 

 

~375,000/cell

 

Ribosomal subunits

 

 

~20000-65000 each per cell

 

mRNAs

 

 

~50000/cell

 

GTP and ATPs

 

 

????

 

 

Ribosome

Remodeling factor-RMF

 

50a.a

 

 

Binds to 50s, Dimerize it; Stalls under stress

Hibernation factor-Hib

 

 

 

 

 

 

Bacteria:

 

rrn rRNA operons:-8-11 operons  

Ribosomal protein coding genes:-6 operons,

~20,000 --70000 ribosomes per cell,(550000-70000),

tRNA: Genes per genome-55.6; ~375,000tRNAs per cell,

mRNA: per cell-~50-60K per cell.

RNAPs:-4600