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Publié par | freie_universitat_berlin |
Publié le | 01 janvier 2010 |
Nombre de lectures | 40 |
Langue | English |
Poids de l'ouvrage | 13 Mo |
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Investigation on the Interaction of Dipeptidyl Peptidase IV
with the Transactivator of Transcription Protein of Human
Immunodeficiency Virus Type-1
Dissertation to achieve the academic degree of
Doctor of Natural Sciences (Dr. rer. nat.)
Submitted to the
Department of Biology, Chemistry and Pharmacy
of the
Freie-Universität Berlin
Presented by
Felista Lemnyui Tansi
from Cameroon
2010
Charité-Universitätsmedizin Berlin
Campus Benjamin Franklin
Institute of Biochemistry and Molecular biology
Arnimallee 22
14195, Berlin-Dahlem
This work was performed under the supervision of Priv. Doz. Dr. Hua Fan
The experimental work was performed from April 2005 to December 2009 in the
Institute of Biochemistry and Molecular biology (AG Reutter / Fan) in Berlin
Part of the work has already been published:
Felista L. Tansi, Véronique Blanchard, Markus Berger, Rudolf Tauber, Werner
Reutter and Hua Fan (2010): Interaction of human dipeptidyl peptidase IV and
human immunodeficiency virus type-1 transcription transactivator in Sf9 cells.
Virology J 7, 267
First Reviewer: Priv. Doz. Dr. Hua Fan
Second Reviewer: Prof. Dr. Rupert Mutzel
Disputation: 11-11-2010 Declaration
I hereby declare that this thesis is the result of my original work carried out at the Institute of
Biochemistry and Molecular biology of the Charité-Universitätsmedizin in Berlin-Dahlem,
Germany. The research was an independent study under the supervision of Priv. Doz. Dr. Hua
Fan. This thesis has never been submitted in part or in whole for a degree at any institution.
References to other sources or people’s work have been duly cited and acknowledged.
Signed by author:
Felista Lemnyui Tansi………………………………………………………………………….
“Dignity consists not in possessing honours, but in the
consciousness that we deserve them“
Aristotle
Dedicated
to
my parents, Juliana and Henry
Thanks for not only giving me life, but also making me realise the sense of
being alive!
and to
my late aunt Angeline and her two daughters, my cousins Emma and
Apolonia
who all died suddenly within 6 weeks.
The shock of learning you left this world together, took my breath away.
Thanks to your love and encouragements while alive, I could pick up from
where you left me and become strong enough to complete the work you so
much wanted me to.
May your souls find perfect peace!
Table of contents | i
Table of Contents
1 Introduction ............................................................................................................................ 1
1.1 The Prolyl Oligo-Peptidase family............................................................................................ 1
1.2 Dipeptidyl Peptidase IV (DPPIV) ............................................................................................. 3
1.2.1 Occurrence and distribution of DPPIV ............................................................... 3
1.2.2 Structure of DPPIV ................................................................................................ 4
1.2.3 Biological functions of DPPIV .............................................................................. 7
1.2.3.1 DPPIV as a serine protease ............................................................................................. 7
1.2.3.2 DPPIV in the immune system....................................................................................... 10
1.2.3.2.1 DPPIV as a co-stimulator in T cell activation .................................................. 11
1.2.3.2.2 DPPIV as a regulator of chemokine function ................................................... 12
1.2.4 DPPIV interaction and binding partners........................................................... 14
1.2.4.1 Adenosine deaminase (ADA) ....................................................................................... 14
1.2.4.2 Collagen and Fibronectin .............................................................................................. 15
1.2.4.3 Plasminogen type-2 ...................................................................................................... 16
+ +1.2.4.4 Kidney Na /H ion exchanger 3 (NHE3) ..................................................................... 18
1.2.4.5 The C-X-C Chemokine Receptor 4 (CXCR4) .............................................................. 18
1.2.4.6 CD45 ............................................................................................................................. 19
1.2.4.7 Mannose-6-phosphate / insulin-like growth factor II receptor ..................................... 20
1.2.4.8 Mannose-binding protein (MBP) .................................................................................. 21
1.2.4.9 Caveolin-1 ..................................................................................................................... 22
1.2.4.10 CARMA1 ...................................................................................................................... 23
1.2.5 DPPIV and Diseases ............................................................................................. 25
1.2.5.1 DPPIV in Diabetes Mellitus Type-2 ............................................................................. 26
1.2.5.2 DPPIV in HIV infection and AIDS .............................................................................. 30
1.2.5.2.1 The HIV1 transactivator of transcription (HIV1-TAT) ................................... 32
1.2.5.2.2 Biological roles and effects of HIV1-TAT on its host ..................................... 34
2 Aim of Work ......................................................................................................................... 38
3 Results I: Expression, Purification and Characterization of TAT protein .................... 39
3.1 Expression and Purification of recombinant TAT proteins in E. coli................................. 39
3.1.1 Purification of GST-TAT-His protein ................................................................ 40
Table of contents | ii
3.1.2 Purification of GST-TAT protein ....................................................................... 42
3.1.3 Purification of His-TAT-His fusion protein....................................................... 43
3.1.4 Purification of TAT protein without fusion tags ............................................... 43
3.1.5 Purification of TAT fusion protein with reagents that prevent protein
aggregation ........................................................................................................................... 45
3.2 Expression and purification of TATGFP in stably transfected CHO cells ........................ 46
3.3 Expression and purification of TAT protein in Sf9 cells ...................................................... 48
3.3.1 Cloning, preparation and analysis of TAT-recombinant baculovirus ............ 48
3.3.2 Expression of recombinant TAT protein in Sf9 cells ........................................ 49
3.3.3 Purification of Sf9-TAT and TATV5His protein from Sf9 cells ...................... 50
Summary I: Expression and purification of recombinant TAT protein......................... 51
3.4 Characterization of purified recombinant TAT protein ...................................................... 52
The purified recombinant TAT protein have low endotoxin levels ................................................... 52
3.4.1 Evaluation of the biological activity of purified recombinant TAT protein ... 52
3.4.1.1 The purified recombinant TAT-protein transactivate the viral LTR promoter ............ 53
3.4.1.2 Purified TAT protein influences CXCR4-localisation in stably transfected cell
lines 54
3.4.1.2.1 Analysis of CXCR4GFP expression in CHO and Hek293 cell lines ............... 54
3.4.1.2.2 Purified TAT protein causes vesicular accumulation of CXCR4GFP ............. 55
3.4.2 Effects of recombinant TAT protein on binding and inhibition of human-
DPPIV 56
3.4.2.1 Recombinant TAT did not bind DPPIV in pull-down, immunoprecipitation or
SPR 56
3.4.2.2 Recombinant TAT retards the cleavage of a chromogenic substrate by DPPIV .......... 56
3.4.2.3 Recombinant TAT retards the cleavage of natural substrates by DPPIV ..................... 58
3.4.2.3.1 Recombinant Sf9-TAT, TAT10xHis and His-TAT-His retard cleavage of
GLP1 by human-DPPIV .................................................................................................... 60
3.4.3 The HIV1-TAT reveal properties typical of intrinsically unstructured proteins
62