Journal of HIV & Retro Virus Open Access

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Commentary - (2021) Volume 7, Issue 3

Short Note on HIV Integration

Lisvaneth Medina*

Department of Neurology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu Province, China

*Corresponding Author:
Lisvaneth Medina
Department of Neurology
The First Affiliated Hospital of Nanjing Medical University
300 Guangzhou Road, Nanjing, Jiangsu Province, China
E-mail: lismedina@gmail.com

Received Date: October 28, 2021; Accepted Date: November 11, 2021; Published Date: November 18, 2021

Citation: Medina L (2021) Short Note on HIV Integration. J HIV Retrovirus Vol.7 No.3:9.

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Description

HIV is a retrovirus, which comprise a large and different family of RNA contagions that make a DNA dupe of their RNA genome after infection of a host cell. An essential step in the replication cycle of HIV-1 and other retroviruses is the integration of this viral DNA into the host DNA. The RNA genome of virions and the template of viral proteins are made when the integrated viral DNA istranscribed HIV-1 Integrase.

Structural Disciplines of the HIV-1 Integrase

The integration of HIV DNA into the host DNA is a critical step in the HIV life cycle. Understanding the integration process will give a frame for gaining sapience into multiple implicit spots of intervention for HIV infection and AIDS. HIV’s enzyme for fitting the DNA interpretation of its genome into the host cell DNA is called its" integrase". HIV-1 integrase catalyses the “cut-andpaste” action of trimming the host DNA and joining the pro viral genome to the cropped ends.

1. Amino (N)-terminal sphere occasionally appertained to as a" zinc cutlet", the N-terminal sphere is composed of the conserved HHCC, His, and Cys remainders, a that serves to bind zinc. The function of the N-terminal sphere isn't fully clear, but is allowed to help the integrase in forming multimers.

2. The central catalytic sphere the catalytic core encompasses the DDE catalytic trio of amino acids, or acid remainders, that manage binding with a divalent essence, forming the active catalytic point. In the case of HIV-1 integrase, the remainders are Asp64, Asp116, and Glu152. This sphere is also well conserved during elaboration.

3. The Car boxy (C)-terminal sphere: The C-terminal sphere on-specifically binds DNA. Since the spots of integration into the target DNA are fairly non-specific, it's allowed that this sphere may work together in some fashion with the target DNA. Crosslinking studies also suggest that the C-terminal sphere works together with a sub terminal region just inside the veritably ends of the viral DNA.

HIV Integrase-Binding Sphere

During the integration process, the HIV integrase enzyme performs two crucial catalytic responses. First is the 3’processing of the HIV DNA, followed by transfer of the HIV DNA into the host DNA. The integration of HIV DNA can do either in dividing or resting cells, and the HIV integrase enzyme can live in the form of a monomer, dimer, tetramer, and conceivably indeed advanced-order forms (similar as octomers). Each has an estimated 40 to 100 clones of the integrase enzyme.

Conclusion

Integrase functions are unique to retroviruses; mortal cells aren't needed to cut-and- paste pieces of DNA into the genome. For this reason, integrase impediments are high targets for developing medicine curatives for HIV infection and AIDS, since inhibition of integrase shouldn't hinder the normal operations in mortal cells.