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Proteomic analysis of HIV-T cell interaction: an update.


ABSTRACT: This mini-review summarizes techniques applied in, and results obtained with, proteomic studies of human immunodeficiency virus type 1 (HIV-1)-T cell interaction. Our group previously reported on the use of two-dimensional differential gel electrophoresis (2D-DIGE) coupled to matrix assisted laser-desorption time of flight peptide mass fingerprint analysis, to study T cell responses upon HIV-1 infection. Only one in three differentially expressed proteins could be identified using this experimental setup. Here we report on our latest efforts to test models generated by this data set and extend its analysis by using novel bioinformatic algorithms. The 2D-DIGE results are compared with other studies including a pilot study using one-dimensional peptide separation coupled to MS(E), a novel mass spectrometric approach. It can be concluded that although the latter method detects fewer proteins, it is much faster and less labor intensive. Last but not least, recent developments and remaining challenges in the field of proteomic studies of HIV-1 infection and proteomics in general are discussed.

SUBMITTER: Kramer G 

PROVIDER: S-EPMC3389432 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

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Proteomic analysis of HIV-T cell interaction: an update.

Kramer Gertjan G   Moerland Perry D PD   Jeeninga Rienk E RE   Vlietstra Wytze J WJ   Ringrose Jeffrey H JH   Byrman Carsten C   Berkhout Ben B   Speijer Dave D  

Frontiers in microbiology 20120704


This mini-review summarizes techniques applied in, and results obtained with, proteomic studies of human immunodeficiency virus type 1 (HIV-1)-T cell interaction. Our group previously reported on the use of two-dimensional differential gel electrophoresis (2D-DIGE) coupled to matrix assisted laser-desorption time of flight peptide mass fingerprint analysis, to study T cell responses upon HIV-1 infection. Only one in three differentially expressed proteins could be identified using this experimen  ...[more]

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