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Chemical Stabilization of the HIV-1 Capsid Results in Efficient HIV-1 Reverse Transcription in vitro

https://doi.org/10.1101/2020.09.17.302315

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/0471142727.mb0214s102openalex-snapshot

DNA Isolation from Mammalian Samples

inferredcites →https://doi.org/10.1002/0471142727.mb0416s103openalex-snapshot

RNA Isolation from Mammalian Samples

inferredcites →https://doi.org/10.1006/meth.1997.0481openalex-snapshot

p24 Antigen Capture Assay for Quantification of Human Immunodeficiency Virus Using Readily Available Inexpensive Reagents

inferredcites →https://doi.org/10.1016/0005-2787(80)90045-3openalex-snapshot

Effects of polyethylene glycol on reverse transcriptase and other polymerase activities

inferredcites →https://doi.org/10.1016/j.bcp.2018.12.011openalex-snapshot

Inositol hexakisphosphate increases the size of platelet aggregates

inferredcites →https://doi.org/10.1016/j.ceb.2010.03.006openalex-snapshot

Inositol phosphate synthesis and the nuclear processes they affect

inferredcites →https://doi.org/10.1016/j.cellsig.2018.01.001openalex-snapshot

Inositol polyphosphates contribute to cellular circadian rhythms: Implications for understanding lithium's molecular mechanism

inferredcites →https://doi.org/10.1016/j.celrep.2019.11.050openalex-snapshot

Cellular IP6 Levels Limit HIV Production while Viruses that Cannot Efficiently Package IP6 Are Attenuated for Infection and Replication

inferredcites →https://doi.org/10.1038/nature09862openalex-snapshot

A conserved mechanism of DEAD-box ATPase activation by nucleoporins and InsP6 in mRNA export

inferredcites →https://doi.org/10.1038/nature19098openalex-snapshot

HIV-1 uses dynamic capsid pores to import nucleotides and fuel encapsidated DNA synthesis

inferredcites →https://doi.org/10.1038/ncb1427openalex-snapshot

Inositol hexakisphosphate and Gle1 activate the DEAD-box protein Dbp5 for nuclear mRNA export

inferredcites →https://doi.org/10.1038/s41564-020-0735-8openalex-snapshot

Nuclear pore blockade reveals that HIV-1 completes reverse transcription and uncoating in the nucleus

inferredcites →https://doi.org/10.1038/s41586-018-0396-4openalex-snapshot

Inositol phosphates are assembly co-factors for HIV-1

inferredcites →https://doi.org/10.1042/bj2890667openalex-snapshot

Comparison of the levels of inositol metabolites in transformed haemopoietic cells and their normal counterparts

inferredcites →https://doi.org/10.1073/pnas.0509996103openalex-snapshot

Specific recognition and accelerated uncoating of retroviral capsids by the TRIM5α restriction factor

inferredcites →https://doi.org/10.1073/pnas.1014522108openalex-snapshot

Complementary assays reveal a relationship between HIV-1 uncoating and reverse transcription

inferredcites →https://doi.org/10.1073/pnas.1419945112openalex-snapshot

Structural basis of HIV-1 capsid recognition by PF74 and CPSF6

inferredcites →https://doi.org/10.1073/pnas.1714361114openalex-snapshot

[PSI+] prion propagation is controlled by inositol polyphosphates

inferredcites →https://doi.org/10.1073/pnas.87.11.4164openalex-snapshot

Integration of human immunodeficiency virus type 1 DNA in vitro.

inferredcites →https://doi.org/10.1093/nar/30.2.e9openalex-snapshot

High-level and high-throughput recombinant protein production by transient transfection of suspension-growing human 293-EBNA1 cells

inferredcites →https://doi.org/10.1097/00002030-199003000-00004openalex-snapshot

Optimal conditions for synthesizing complementary DNA in the HIV-1 endogenous reverse transcriptase reaction

inferredcites →https://doi.org/10.1099/0022-1317-76-7-1675openalex-snapshot

Stepwise analysis of reverse transcription in a cell-to-cell human immunodeficiency virus infection model: kinetics and implications

inferredcites →https://doi.org/10.1101/cshperspect.a006882openalex-snapshot

HIV-1 Reverse Transcription

inferredcites →https://doi.org/10.1126/science.1078068openalex-snapshot

Modulation of ATP-Dependent Chromatin-Remodeling Complexes by Inositol Polyphosphates

inferredcites →https://doi.org/10.1128/jvi.00289-17openalex-snapshot

Reverse Transcription Mechanically Initiates HIV-1 Capsid Disassembly

inferredcites →https://doi.org/10.1128/jvi.00845-18openalex-snapshot

PF74 Reinforces the HIV-1 Capsid To Impair Reverse Transcription-Induced Uncoating

inferredcites →https://doi.org/10.1128/jvi.01406-10openalex-snapshot

Small-Molecule Inhibition of Human Immunodeficiency Virus Type 1 Infection by Virus Capsid Destabilization

inferredcites →https://doi.org/10.1128/jvi.01741-18openalex-snapshot

PF74 Inhibits HIV-1 Integration by Altering the Composition of the Preintegration Complex

inferredcites →https://doi.org/10.1128/jvi.01808-07openalex-snapshot

Cell Factors Stimulate Human Immunodeficiency Virus Type 1 Reverse Transcription In Vitro

inferredcites →https://doi.org/10.1128/jvi.03116-15openalex-snapshot

Roles of Capsid-Interacting Host Factors in Multimodal Inhibition of HIV-1 by PF74

inferredcites →https://doi.org/10.1128/jvi.05811-11openalex-snapshot

RING Domain Mutations Uncouple TRIM5α Restriction of HIV-1 from Inhibition of Reverse Transcription and Acceleration of Uncoating

inferredcites →https://doi.org/10.1128/jvi.65.4.1952-1959.1991openalex-snapshot

Equine infectious anemia virus and human immunodeficiency virus DNA synthesis in vitro: characterization of the endogenous reverse transcriptase reaction

inferredcites →https://doi.org/10.1128/jvi.66.11.6547-6554.1992openalex-snapshot

Macrophage-tropic human immunodeficiency virus isolates from different patients exhibit unusual V3 envelope sequence homogeneity in comparison with T-cell-tropic isolates: definition of critical amino acids involved in cell tropism

inferredcites →https://doi.org/10.1128/jvi.71.8.5871-5877.1997openalex-snapshot

Pseudotyping human immunodeficiency virus type 1 (HIV-1) by the glycoprotein of vesicular stomatitis virus targets HIV-1 entry to an endocytic pathway and suppresses both the requirement for Nef and the sensitivity to cyclosporin A

inferredcites →https://doi.org/10.1128/jvi.75.8.3626-3635.2001openalex-snapshot

Characterization of Intracellular Reverse Transcription Complexes of Human Immunodeficiency Virus Type 1

inferredcites →https://doi.org/10.1128/jvi.76.11.5667-5677.2002openalex-snapshot

Formation of a Human Immunodeficiency Virus Type 1 Core of Optimal Stability Is Crucial for Viral Replication

inferredcites →https://doi.org/10.1128/jvi.80.8.3712-3720.2006openalex-snapshot

Evidence for a Functional Link between Uncoating of the Human Immunodeficiency Virus Type 1 Core and Nuclear Import of the Viral Preintegration Complex

inferredcites →https://doi.org/10.1186/1742-4690-10-29openalex-snapshot

The NTD-CTD intersubunit interface plays a critical role in assembly and stabilization of the HIV-1 capsid

inferredcites →https://doi.org/10.1186/1742-4690-9-30openalex-snapshot

Second-site suppressors of HIV-1 capsid mutations: restoration of intracellular activities without correction of intrinsic capsid stability defects

inferredcites →https://doi.org/10.1371/journal.ppat.1004459openalex-snapshot

Host Cofactors and Pharmacologic Ligands Share an Essential Interface in HIV-1 Capsid That Is Lost upon Disassembly

inferredcites →https://doi.org/10.3791/3384openalex-snapshot

In vitro Uncoating of HIV-1 Cores

inferredcites →https://doi.org/10.7554/elife.04114openalex-snapshot

Quantitative microscopy of functional HIV post-entry complexes reveals association of replication with the viral capsid

inferredcites →https://doi.org/10.7554/elife.35335openalex-snapshot

IP6 is an HIV pocket factor that prevents capsid collapse and promotes DNA synthesis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1371/journal.ppat.1009190openalex-snapshot

Inositol phosphates promote HIV-1 assembly and maturation to facilitate viral spread in human CD4+ T cells

inferred← citeshttps://doi.org/10.5772/intechopen.1017525openalex-snapshot

Molecular Mechanisms of Viral Genome Replication During Infection

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