Authors

Lu Bai

Type

Text

Type

Thesis

Advisor

London, Erwin. | Seeliger, Jessica | Tonge, Peter

Date

2013-12-01

Keywords

Chemistry

Department

Department of Chemistry.

Language

en_US

Source

This work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.

Identifier

http://hdl.handle.net/11401/77086

Publisher

The Graduate School, Stony Brook University: Stony Brook, NY.

Format

application/pdf

Abstract

Two lipoproteins, MtbLprG and MtbLprA, have been characterized as TLR2 agonists. Knockout of the lprG operon (lprG-rv1410c) results in decreased virulence of M. tb. While their importance for host-pathogen interactions has been the subject of numerous studies, the physiological functions of LprG and LprA are not known. We present here data towards elucidating the physiological functions of LprG and LprA, both in M. tb and M. smegmatis, including localization, binding affinity to respective ligands, as well as the phenotype of knockout strains, which will contribute a model for lipid transport through the cell wall. | 46 pages

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