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|Title: ||FTSZ INHIBITION: A PROMISING APPROACH FOR ANTI-STAPHYLOCOCCAL THERAPY|
|Authors: ||SINGH, P|
|Keywords: ||cell-division protein|
|Issue Date: ||2010|
|Publisher: ||PROUS SCIENCE, SA-THOMSON REUTERS|
|Citation: ||DRUG NEWS & PERSPECTIVES, 23(5), 295-304|
|Abstract: ||Staphylococcus causes a large number of animal and human diseases and has been considered as a major health concern. With the emergence of resistant strains of staphylococcus, like methicillin-resistant Staphylococcus aureus and vancomycin-resistant Staphylococcus aureus, the search for novel antibacterial targets has intensified. FtsZ, a bacterial cytoskeleton protein, is involved in cell division. FtsZ assembles into protofilaments in a GTP-dependent manner, and forms a dynamic Z-ring at the mid-cell position. The assembly dynamics of FtsZ in the Z-ring are regulated by the combined actions of several FtsZ-associated proteins. Furthermore, the interaction of FtsZ with accessory proteins is essential for their recruitment to the Z-ring. A disruption of this interaction perturbs the Z-ring formation. FtsZ inhibitors like PC-190723 have been suggested to inhibit the Staphylococcus cell division by perturbing the assembly and stabitity of FtsZ polymers. In this review, we discuss the assembly dynamics of Z-ring and its role in cell division. In addition, we highlight recent advances suggesting the potential of FtsZ as a drug target for antistaphylococcal therapy.|
|Appears in Collections:||Article|
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