2018-07-16l Hit 2376
The competition between bacteria and viruses (bacteriophages) has taken place on this planet since long before the dawn of mankind. Ever since the beginning of their symbiosis, viral infection and bacterial defense mechanisms have grown more and more sophisticated with one evolving after the other, solely in the interest of survival. Scientists have long endeavored to understand the molecular machineries operating in the battle between bacteria and virus. With the help of recent progress in scientific techniques, our understanding of the interaction between bacteria and viruses is ever increasing. This includes the recent discovery of anti-스피드 바카라 proteins.
To understand what anti-스피드 바카라 is, we first introduce 스피드 바카라. 스피드 바카라 stands for “clustered regularly interspaced short palindromic repeat”. 스피드 바카라 consists of short genetic sequences of viral origin, followed by various genetic architecture that expresses Cas (스피드 바카라-associated) protein within bacteria. These proteins act as an immune surveillance system to counteract viruses that infect the bacteria by remembering the virus genome and destroying viral DNA/RNA by the RNA-guided endonucleases. 스피드 바카라 has been widely utilized as one of the most powerful gene editing tools with enormous potential, albeit cautions remain due to the uncontrollable and perilous side effects. This is where anti-스피드 바카라 kicks in as a potential regulator for 스피드 바카라 proteins.
Anti-스피드 바카라 is a defense mechanism within a virus to evade the bacterial immune system. Proteins expressed from the anti-스피드 바카라 gene bind to Cas proteins and prevent it from destroying the viral genome. This viral defense system could act as an off-switch for genome editing to avoid unexpected off-target consequences. So apart from constituting the viral defense system, anti-스피드 바카라 promises a useful tool that could potentially increase the efficiency and elaborateness of gene editing.
Only a few types of anti-스피드 바카라 proteins have been found so far, and professors Jeong-Yong Suh and Euiyoung Bae (Department of Agricultural Biotechnology, Seoul National University) led their research team to first unveil the structure of the anti-스피드 바카라 protein AcrIIA1using X-ray crystallography. AcrIIA1 forms a dimer with the N-terminal domain exhibiting a helix-turn-helix (HTH) motif that resembles transcriptional factors. The HTH motif is generally known to participate in the DNA-binding, but AcrIIA1 exhibits an RNA-binding affinity instead, making it an unconventional type of 스피드 바카라-Cas inhibition mechanism. The study also proposed the possibility that AcrIIA1’s C-terminal domain may function through interaction with other proteins.
With this breakthrough, we now know that an anti-스피드 바카라 protein can bind directly with nucleic acids, expanding the current mechanism that they interact with different types of Cas proteins. This suggests that the defense mechanism of 스피드 바카라 and anti-스피드 바카라 may be more involved than originally believed and opens up new possibilities for further research. Scientists have been chasing the dream of taking full control over gene editing for decades. We are learning more and more about the world invisible to naked eyes, filling the gap between the prediction and the reality. With the exponential growth in the advancement of science, it is foreseeable that the dreams of many years may come true in near future, providing the personalized medicine for genetic diseases on demand.
By Jun Soo Kim / HyungChul Nam
Students reporters, CALS