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J Mol Model ; 18(1): 27-37, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21445708

RESUMO

The Galanthus nivalis agglutinin (GNA)-related lectin family exhibit significant anti-HIV and anti-HSV properties that are closely related to their carbohydrate-binding activities. However, there is still no conclusive evidence that GNA-related lectins possess anti-influenza properties. The hemagglutinin (HA) of influenza virus is a surface protein that is involved in binding host cell sialic acid during the early stages of infection. Herein, we studied the 3D-QSARs (three-dimensional quantitative structure-activity relationships) of lectin- and HA-sialic acid by molecular modeling. The affinities and stabilities of lectin- and HA-sialic acid complexes were also assessed by molecular docking and molecular dynamics simulations. Finally, anti-influenza GNA-related lectins that possess stable conformations and higher binding affinities for sialic acid than HAs of human influenza virus were screened, and a possible mechanism was proposed. Accordingly, our results indicate that some GNA-related lectins, such as Yucca filamentosa lectin and Polygonatum cyrtonema lectin, could act as drugs that prevent influenza virus infection via competitive binding. In conclusion, the GNA-related lectin family may be helpful in the design of novel candidate agents for preventing influenza A infection through the use of competitive combination against sialic acid specific viral infection.


Assuntos
Vírus da Influenza A Subtipo H1N1/efeitos dos fármacos , Lectinas de Ligação a Manose/química , Modelos Moleculares , Simulação de Dinâmica Molecular , Lectinas de Plantas/química , Sequência de Aminoácidos , Antivirais/química , Ligação de Hidrogênio , Modelos Químicos , Dados de Sequência Molecular , Estrutura Secundária de Proteína , Relação Quantitativa Estrutura-Atividade , Alinhamento de Sequência , Análise de Sequência de Proteína
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