Faculty Advisor

Adams, David S.

Abstract

HIV-1 uses specific cell surface receptors to gain entry into host cells. Different strains vary in ability to infect cells with low receptor concentrations. The MQP's purpose was to analyze molecular clones of an HIV variant that had broad tropism for immune cells. These clones were tested for their ability to fuse with cells expressing known receptor concentrations. The data shows that this HIV variant was more fusiogenic for cells with low receptor expression than the wild type strain.

Publisher

Worcester Polytechnic Institute

Date Accepted

April 2005

Major

Biology and Biotechnology

Project Type

Major Qualifying Project

Accessibility

Unrestricted

Advisor Department

Biology and Biotechnology

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