Exam 4 Quiz 3 Flashcards
making protein involves
all 3 forms of RNA: mRNA, tRNA, rRNA
mRNA
-uses the genetic code as their language
-reads as a series of triplets called codons
-each codon codes for a specific amino acid
how many possible codons
64
how many amino acids
20
genetic code redundancy
more than 1 codon can code for the same amino acid
wobble site
third site within the codon because it is not needed to define the amino acid
start site
AUG
stop codons
UAG
UAA
UGA
why is reading frame important
the movement or shift down of only one codon can change the amino acid that it codes for changing the genetic code
AUG in bacteria contains
formyl methionine
tRNA
-transfer RNA
-73-93 nucleotides long
-single stranded with secondary structures
-modified bases
why does tRNA have increased stability when compared to mRNA
through the single strands with secondary structures and the modified bases
modified bases
pseudouridine, inosine, D=dihydrouridine, dimethyl guanosine
clover leaf structure
structure of tRNA that is beneficial in that it prevents attack by ribonuclease becasue they typically attacked linear
what forms the clover leaf structure
intra-strand base pairing
functional importance of tRNA
-anti-codon area
-3’ acceptor end
anti codon area
bases that recognize mRNA codons
3’ acceptor end
-attaches 3 bases (cytosine, cytosine, adenine) to 3’ end
-termed CCA
what adds CCA onto the 3’ end
CCA adding enzyme
aminoacyl-tRNA synthase
adds amino acid onto the CCA
rRNA
prime component of ribosomes
ribosomes
-where translation occurs
-site of protein synthesis
-60% rRNA
-40% protein
prokaryotic ribosomal subunits
70S total, 50S large, 30S small
eukaryotic ribosomal subunits
80S total, 60S large, 40S small
rRNA off of 50S subunit
5S and 23S rRNA
rRNA off of 30S subunit
16S rRNA
rRNA off of 60S subunit
5S, 5.8S, and 28S rRNA
rRNA off of 40S subunit
18S rRNA
translation initiation
small subunit is separated from large subunit
what keeps the two subunits separated
IF-3 initiation factor that is bound to the 30S subunit
5’ untranslated region upstream of a gene has…
…Shine dalgarno sequence
Shine Dalgarno sequence
base pairs with the 3’ end of the 16S rRNA which puts AUG into prime recognition
when AUG is in prime recognition then
AUG becomes available for recognition by the tRNA carriers: formyl methionine
what helps tRNA get into its place
IF-2
where does tRNA eventually need to get into
future P site
what is displaced that causes initiation
IF-1 displaces IF-3 which begins the process of initiation
when initiation begins, what is opened up
50S subunit is open, IF-2 then uses energy to pack the tRNA into the P site and then leaves
where do all incoming tRNA go?
A site, except tRNA 1 goes to P site
elongation factors
-EF-Tu
-EF-Ts
-23S rRNA
-EF-G
EF-Tu
-helps bring in next tRNA with amino acid
-if it fits anticodon loop then 16S + 23S interact and GTP locks in place
-GTP becomes GDP
EF-Ts
turns GDP back into GTP
23S rRNA
-peptidyl transferase enzyme
-RNA based
-binds AA in P site
-needs translation to occur in order to shift ribosome down 1 unit (requires energy)
EF-G
-helps move the ribosome down a unit
-moves empty tRNA from P site to E site (to exit)
-growing peptide then moves into P site to have empty A site to start process over again
why is translation efficient
-polycistronic sequences
-multiple ribosomes can attach because of trasnlocation
polysomes
makes translation more efficient
**not speific to eukaryotes
polysomes in prokaryotes
-combine transcription and translation to occur simultaneously
why can transcription and translation occur at the same time in eukaryotes?
-they have no nucleus
-RNA polymerase
protein folding uses…
-chaperones
-GroEL
-GroES
chaperone proteins
-initiate folding
-DNA K and DNA J are the main mechanisms used
DNA K and DNA J
ATP dependent enzymes
GroEL and GroES
make up a barrel structure that allows the protein to go through which forces proper protein folding (ATP dependent)
protein processing first codon
-first codon typically cleaved away BUT bactera tend to not cleave off all of their protein
what is left behind when bacteria doesnt cleave off all protein
formyl methionine
formyl methionine is
a great trigger four our immune response
why is formyl methionine a trigger for our immune response
our white blood cells ahve formyl methionine receptors to fight off/start an immune response against it
after prtein get made they go through
extra processing in the ER and golgi to attach sugars
glycosylation
sugaring process
most antibiotics are derived from
bacteria
antibiotics that inhibit protein synthesis
-Aminoglycosides
-Tetracyclines
-Chloramphenicol
-Macrolides
what do all of those antibiotics target?
70S ribosome which is only effective against bacteria
how to we prevent the antibiotics from attacking the 70S in our mitochondria
by giving the antibiotic in smaller concentration doses so it does not interfere
Aminoglycosides
-obtained from streptomyces
-streptomycin, gentamycin, tobramycin, neomycin
-cyclohexane ring and 1 or more amino sugars
-binds to 30S causing misreading of mRNA message
-effective against gram - enteric
-bacteriocidial
bacteriocidial
kill microorgansims
bacteriostatic
prevent reproduction of microorganisms
Tetracyclines
-broad spectrum
-binds to 30S and inhibits enterance of tRNA onto A site
-not used in kids or pregnant women
-acne medicine and animal feel
-bacteriostatic
chloramphenicol
-broad spectrum
-obtained from streptomyces venezuelae
-binds to 50S inhibits formation of peptide binds between AA
-last resort antibiotic bc of bad side effects
-used in 3rd world countries
side effects of chloramphenicol
aplastic anemia: low white, red, and platelet count which messes with bone marrow production
macrolides
-erythromycin, clarithromycin, azithromycin
-lactone rings to one or more sugars
-binds to 50S ribosomal subunit + prevents translocation of the ribosome: EFG is responsible
bacteria timing of transcription and translation
same time
eukarya timing of transcription and translation
sperate time
archaea timing of transcription and translation
seperate time
bacteria recognition of mRNA by small ribosomal subunit
shine dalgarno sequence
eukarya recognition of mRNA by small ribosomal subunit
5’ cap
archaea recognition of mRNA by small ribosomal subunit
shine dalgarno sequence
bacteria coding of start codon
formyl methionine
eukarya coding of start codon
AUG mehtionine
archaea coding of start codon
AUG methionine
bacteria amount of transcription factors
fewest
eukarya amount of transcription factors
multi-subunit, a lot more complex
archaea amount of transcription factors
multi subunit but not complex
bacteria amount of termination factors
3
eukarya amount of termination facotrs
1
archaea amount of termination factors
1