• No results found

University of Groningen The oligomeric protein interference assay method for validation of antimalarial targets de Assis Batista, Fernando

N/A
N/A
Protected

Academic year: 2021

Share "University of Groningen The oligomeric protein interference assay method for validation of antimalarial targets de Assis Batista, Fernando"

Copied!
2
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

The oligomeric protein interference assay method for validation of antimalarial targets

de Assis Batista, Fernando

DOI:

10.33612/diss.94898872

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date: 2019

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

de Assis Batista, F. (2019). The oligomeric protein interference assay method for validation of antimalarial targets. University of Groningen. https://doi.org/10.33612/diss.94898872

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)

Propositions

accompanying the thesis

T

HE

O

LIGOMERIC

P

ROTEIN

I

NTERFERENCE

A

SSAY

M

ETHOD FOR

V

ALIDATION OF

A

NTIMALARIAL

T

ARGETS by

Fernando A. B

ATISTA

1. The significant limitations found in the current antimalarial target validation tool set highlight the need for novel specific validation techniques (this thesis). 2. Oligomeric interface disruption can be achieved by the introduction of mutant

subunits in oligomeric protein complexes (this thesis).

3. Manipulation of oligomeric surfaces allow for control of specific enzyme activity in vitro and in vivo (this thesis).

4. Oligomeric surfaces possess a high potential to be explored in the validation of essential oligomeric enzymes of Plasmodium parasites (this thesis).

5. The oligomeric protein interference assay (PIA) is a minimally perturbing method to specifically inhibit metabolic pathways of interest with a minimal off-target effect (this thesis).

6. Enzymes integral to the aspartate biosynthetic pathway of Plasmodium falciparum are promising targets for the discovery of novel antimalarials (this thesis).

7. Learning how to keep the excitement in frustration might be the most important skill you will learn during your PhD (my view).

8. Ideas are like rabbits. You get a couple and learn how to handle them, and pretty soon you have a dozen (John Steinbeck).

9. Succes is soms het resultaat van een hele reeks mislukkingen (Vincent van Gogh).

Referenties

GERELATEERDE DOCUMENTEN

Drug Target Validation Methods in Malaria - Protein Interference Assay (PIA) as a Tool for Highly Specific Drug Target Validation, Current Drug Targets 18, 9, p... Identification

Development of novel anticancer agents for protein targets Estrada Ortiz, Natalia.. IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish

Additionally, a series of gold complexes were studied to understand their possible mechanism of action compared with cisplatin, including cancer cell based studies and healthy

The cytotoxic activities of the compounds were tested in 4 human cancer cell lines and their toxicity in healthy tissue was determined using rat precision cut kidney slices as a

Crystal structure of compound 3 (WK23) bound to MDM2 (PDB: 3LBK): A hydrogen bond between the indole N-H of 3 and the MDM2 Leu54 carbonyl oxygen is depicted.. The

The organic layer was separated, washed with water, dried over anhydrous MgSO 4 and evaporated, affording the corresponding compounds 1 (yields 11-ϳϬйͿ. as a

To a stirred solution of the corresponding compounds 2 (1.0 mmol) in EtOH-water (1:1), LiOH (10.0 mmol) was added and the reaction mixture refluxed overnight.. Then, pH was adjusted

In the present study, the potential selectivity of these compounds was studied in an ex-vivo model, using rat precision cut kidney and liver slices (PCKS and PCLS), to determine