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Biochemical and biophysical analyses of concerted (U5/U3) integration. | LitMetric

Biochemical and biophysical analyses of concerted (U5/U3) integration.

Methods

Saint Louis University Health Sciences Center, Institute for Molecular Virology, Doisy Research Center, Rm 621, 1100 South Grand, St. Louis, MO 63104-1009, USA.

Published: April 2009

AI Article Synopsis

  • Retrovirus integrase (IN) is crucial for the replication of viruses like HIV-1 by integrating viral DNA into host chromosomes through a preintegration complex (PIC).
  • This article discusses methods to recreate synaptic complexes that reflect the PIC's properties, allowing for the study of how IN interacts with viral DNA and other proteins at a molecular level.
  • The techniques described enable investigations into IN's function, resistance to inhibitors, and implications for treating HIV/AIDS, including analyzing the relationships between IN and cellular proteins.

Article Abstract

Retrovirus integrase (IN) integrates the viral linear DNA genome ( approximately 10 kb) into a host chromosome, a step which is essential for viral replication. Integration occurs via a nucleoprotein complex, termed the preintegration complex (PIC). This article focuses on the reconstitution of synaptic complexes from purified components whose molecular properties mirror those of the PIC, including the efficient concerted integration of two ends of linear viral DNA into target DNA. The methods described herein permit the biochemical and biophysical analyses of concerted integration. The methods enable (1) the study of interactions between purified recombinant IN and its viral DNA substrates at the molecular level; (2) the identification and characterization of nucleoprotein complexes involved in the human immunodeficiency virus type-1 (HIV-1) concerted integration pathway; (3) the determination of the multimeric state of IN within these complexes; (4) dissection of the interaction between HIV-1 IN and cellular proteins such as lens epithelium-derived growth factor (LEDGF/p75); (5) the examination of HIV-1 Class II and strand transfer inhibitor resistant IN mutants; (6) the mechanisms associated with strand transfer inhibitors directed against HIV-1 IN that have clinical relevance in the treatment of HIV-1/AIDS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2693883PMC
http://dx.doi.org/10.1016/j.ymeth.2008.11.002DOI Listing

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