The Furin Protease Dependence and Antiviral GBP2 Sensitivity of Murine Leukemia Virus Infection Are Determined by the Amino Acid Sequence at the Envelope Glycoprotein Cleavage Site
Abstract
:1. Introduction
2. Results
2.1. GBP2 Does Not Inhibit Transduction by Amphotropic MLV-Pseudotyped HIV-1 Vector
2.2. X-MLV and A-MLV Are Resistant to GBP2, but E-MLV and P-MLV Are Susceptible
2.3. The Susceptibility of GBP2 Is Determined by the Amino Acid Sequence at the SU-TM Cleavage Site
2.4. The Susceptibility to Furin Silencing Is Determined by the Amino Acid Sequence at the SU-TM Cleavage Site
2.5. Amino Acid Sequences at the SU-TM Cleavage Sites of Different MLVs
3. Discussion
4. Materials and Methods
4.1. Cells
4.2. A-MLV-Pseudotyped HIV-1-Based Vector
4.3. MLV-Based Vector
4.4. Western Blotting
4.5. Site-Directed Mutagenesis
Primers | Nucleotide Sequences |
---|---|
E-MLV FM | CTG TTT GAG AGA AAA ACC AAA TAT AAA AGA GAG CCG |
X-MLV FM | CAA TTT GAG AGA AGC AAC AGA CAT AAA AGA GAG CCG |
5. Conclusions
Author Contributions
Funding
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Kubo, Y.; Hans, M.B.; Nakamura, T.; Hayashi, H. The Furin Protease Dependence and Antiviral GBP2 Sensitivity of Murine Leukemia Virus Infection Are Determined by the Amino Acid Sequence at the Envelope Glycoprotein Cleavage Site. Int. J. Mol. Sci. 2024, 25, 9987. https://doi.org/10.3390/ijms25189987
Kubo Y, Hans MB, Nakamura T, Hayashi H. The Furin Protease Dependence and Antiviral GBP2 Sensitivity of Murine Leukemia Virus Infection Are Determined by the Amino Acid Sequence at the Envelope Glycoprotein Cleavage Site. International Journal of Molecular Sciences. 2024; 25(18):9987. https://doi.org/10.3390/ijms25189987
Chicago/Turabian StyleKubo, Yoshinao, Manya Bakatumana Hans, Taisuke Nakamura, and Hideki Hayashi. 2024. "The Furin Protease Dependence and Antiviral GBP2 Sensitivity of Murine Leukemia Virus Infection Are Determined by the Amino Acid Sequence at the Envelope Glycoprotein Cleavage Site" International Journal of Molecular Sciences 25, no. 18: 9987. https://doi.org/10.3390/ijms25189987