4.6 Article

Broad-spectrum anti-human immunodeficiency virus (HIV) potential of a peptide HIV type 1 entry inhibitor

期刊

JOURNAL OF VIROLOGY
卷 81, 期 7, 页码 3645-3648

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AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.01778-06

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资金

  1. NIAID NIH HHS [R21 AI 071265-01] Funding Source: Medline
  2. NIGMS NIH HHS [P01 GM056550, P01 GM 056550-08] Funding Source: Medline
  3. NINDS NIH HHS [R21 NS047970] Funding Source: Medline
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [Z01AI000883, Z01AI000887] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [P01GM056550] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R21NS047970] Funding Source: NIH RePORTER

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The AIDS epidemic continues to spread at an alarming rate worldwide, especially in developing countries. One approach to solving this problem is the generation of anti-human immunodeficiency virus (HIV) compounds with inhibition spectra broad enough to include globally prevailing forms of the virus. We have examined the HIV type 1 (HIV-1) envelope specificity of a recently identified entry inhibitor candidate, UNG-105, using surface plasmon resonance spectroscopy and pseudovirus inhibition assays. The combined results suggest that the HNG-105 molecule may be effective across the HIV-1 subtypes, and they highlight its potential as a lead for developing therapeutic and microbicidal agents to help combat the spread of AIDS.

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