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1.
Nat Struct Mol Biol ; 30(3): 383-390, 2023 03.
Artigo em Inglês | MEDLINE | ID: mdl-36759579

RESUMO

The HIV-1 capsid is a fullerene cone made of quasi-equivalent hexamers and pentamers of the viral CA protein. Typically, quasi-equivalent assembly of viral capsid subunits is controlled by a molecular switch. Here, we identify a Thr-Val-Gly-Gly motif that modulates CA hexamer/pentamer switching by folding into a 310 helix in the pentamer and random coil in the hexamer. Manipulating the coil/helix configuration of the motif allowed us to control pentamer and hexamer formation in a predictable manner, thus proving its function as a molecular switch. Importantly, the switch also remodels the common binding site for host factors that are critical for viral replication and the new ultra-potent HIV-1 inhibitor lenacapavir. This study reveals that a critical assembly element also modulates the post-assembly and viral replication functions of the HIV-1 capsid and provides new insights on capsid function and inhibition.


Assuntos
Capsídeo , HIV-1 , Capsídeo/química , HIV-1/química , Proteínas do Capsídeo/química
2.
Curr Protoc Cytom ; 70: 12.36.1-10, 2014 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-25271959

RESUMO

Correlative fluorescence and electron microscopy (CFEM) is a multimodal technique that combines dynamic and localization information from fluorescence methods with ultrastructural data from electron microscopy, to give new information about how cellular components change relative to the spatiotemporal dynamics within their environment. In this review, we will discuss some of the basic techniques and tools of the trade for utilizing this attractive research method, which is becoming a very powerful tool for biology labs. The information obtained from correlative methods has proven to be invaluable in creating consensus between the two types of microscopy, extending the capability of each, and cutting the time and expense associated with using each method separately for comparative analysis. The realization of the advantages of these methods in cell biology has led to rapid improvement in the protocols and has ushered in a new generation of instruments to reach the next level of correlation--integration.


Assuntos
Microscopia Eletrônica/instrumentação , Microscopia Eletrônica/métodos , Animais , Humanos , Microscopia de Fluorescência/instrumentação , Microscopia de Fluorescência/métodos
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