After budding from the cell, retroviruses (such as HIV) undergo a complex spontaneous process called maturation that is required for their infectivity. During maturation retroviruses undergo dramatic internal reorganization. These changes have been extensively characterized in HIV by biochemical and electron microscopy methods. Very recently, atomic force microscopy (AFM) measurements have revealed a dramatic decrease in virion stiffness during maturation (""""""""stiffness switch""""""""). Interestingly, this stiffness switch is largely controlled by the viral envelope (Env) protein, which also mediates the ability of virions to enter target cells. The proposed studies will dissect the mechanism of the HIV stiffness switch and determine how Env regulates this switch. Current data suggests a correlation between virion stiffness and entry activity. The proposed studies will also determine if viral mechanical properties directly control viral entry activity. Such a novel regulatory mechanism would reveal a previously unappreciated layer of complexity in the retrovirus life-cycle and will have broader implications for mechanical regulation of other complex biological systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI076735-01
Application #
7360356
Study Section
Macromolecular Structure and Function C Study Section (MSFC)
Program Officer
Salzwedel, Karl D
Project Start
2009-06-01
Project End
2011-05-31
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
1
Fiscal Year
2009
Total Cost
$220,438
Indirect Cost
Name
University of Utah
Department
Biochemistry
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Pang, Hong-Bo; Hevroni, Liron; Kol, Nitzan et al. (2013) Virion stiffness regulates immature HIV-1 entry. Retrovirology 10:4
Kol, Nitzan; Tsvitov, Marianna; Hevroni, Liron et al. (2010) The effect of purification method on the completeness of the immature HIV-1 Gag shell. J Virol Methods 169:244-7