Protein synthesis inhibitors:
- Protein synthesis inhibitors are substances that prevent
protein synthesis by inactivating components required for
proteinsynthasis or preveinting elongation or formation of
polypeptide chains.
- Antibiotics like Tetracycline, Chloramphenicol, act as protein
synthesis inhibitors.
- The antibiotics which inhibit protein synthesis, should
essentially inhibit the pathogen (bacteria) protein synthesis.
- The inhibitor may prevent initiation of protein synthesis by
preventing formation of initiation complex in bacteria. Like
Neomycin.
- Antibiotics acting as protein synthesis inhibitors specifically
select 70s ribosomal subunit of bacteria and do not inhibit the
eukaryotic 80 s ribosomal subunit. Thus, peptidyl transferase
activity is prevented. Like Chloramphenicol.
- Some may block the A site, preventing the entry of Amino-acyl
tRNA. Like Tetracycline.
- Other methods include, preventing formation of ribosomal
assembly, inhibiting ribosomal translocation, translation
termination inhibition.
DNA synthesis inhibitors:
- DNA synthesis inhibitors are compounds that prevent DNA
replication or components that are involved in the nucleic acid
generation.
- DNA synthesis inhibitors may inhibit action of DNA gyrase, like
fluoroquinolones.
- Chain elongation may be prevented by inhibitors like Cisplatin,
MMS.
- Inhibiting CDKs or checkpoints may affect ori site, like by
Flavopyridol.
- Chain elongation during replication may be prevented by
Acyclovir.
Antimycobacterium antibiotics:
- Mycobacterium cell has a waxy coat, containing mycolic acid,
which make it impervious to Gram staining. Their cell wall contains
high proportion of high-molecular-weight lipids. They may
unpredictably acquire Gram positive or negative
characteristics.
- Tuberculosis or TB is a contagious infection affecting majorly
lungs, may spread to brain, spinal cord.
- The causal microorganism is a bacterium, called Mycobacterium
tuberculosis (orMycobacterium bovis, Mycobacterium africanum, of
the same family).
- Thus, the antimycobacterial drugs needs to penetrate the
hydrophobic mycolic acid layer.
-
Two common antomycobacterium drugs are resorcinomycin and
pheganomycin.
-
These drugs have hydrophobic lipid layers that help in their
penetration through mycobacterium wall.
-
Also Urydyl-peptide antibiotics like Rifampicin and Isoniazid
can form pore in these bacterial membranes.