• No results found

N -acylethanolamine biosynthesis with new chemical tools Illuminating

N/A
N/A
Protected

Academic year: 2021

Share "N -acylethanolamine biosynthesis with new chemical tools Illuminating"

Copied!
6
0
0

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

Hele tekst

(1)

Illuminating N-acylethanolamine biosynthesis

with new chemical tools

PROEFSCHRIFT

ter verkrijging van

de graad van Doctor aan de Universiteit Leiden, op gezag van Rector Magnificus prof. mr. C.J.J.M. Stolker,

volgens het besluit van het College voor Promoties te verdedigen op woensdag 6 november 2019

klokke 15:00 uur

door

Elliot David Mock

(2)

2

Promotiecommissie

Promotores: Prof. dr. M. van der Stelt Prof. dr. C.A.A. van Boeckel

Overige leden: Prof. dr. H.S. Overkleeft Prof. dr. J.M.F.G. Aerts Prof. dr. C.J. Hillard

Medical College of Wisconsin, USA

Prof. dr. C.J. Schofield

Oxford University, UK

Dr. G.J.P. van Westen

(3)
(4)
(5)

Table of contents

Chapter 1 7

Therapeutic opportunities of modulating the endogenous N-acylethanolamine tone

Chapter 2 45

High-throughput screening delivers new inhibitors for NAPE-PLD

Chapter 3 63

Optimization of pyrimidine-4-carboxamide NAPE-PLD inhibitors affords LEI-401

Chapter 4 131

Photoaffinity probes for NAPE-PLD confirm LEI-401 target engagement Chapter 5 175

LEI-401 is an in vivo active NAPE-PLD inhibitor that reduces brain anandamide levels and pain behavior Chapter 6 201

Discovery and optimization of -ketoamide inhibitors for the N-acyltransferase PLAAT2 Chapter 7 239

Summary and future prospects Nederlandse Samenvatting 264

List of publications 272

Curriculum Vitae 274

(6)

Referenties

GERELATEERDE DOCUMENTEN

succeeded in introducing amino acids with unsaturated side chains (for instance, 2-amino-5-hexynoic acid) into proteins. 12 In a joint effort of the Tirrell and Bertozzi groups,

irreversible proteasome inhibition and subsequent Staudinger ligation- mediated biotinylation to enable visualization of proteasomes in an activity- based manner.

Activity probe 5 allows two step labeling of active caspase-like subunits of the immunoproteasome and, at higher concentrations, of the constitutive proteasome.. Labeled subunits

10, 11 A relevant example of a chemical proteomics probe is represented by 1a (DCG-04, Figure 1), developed by Bogyo and coworkers as an irreversible cysteine protease inhibitor,

As a model for the dialysis of 1, ovalbumin was incubated with DCG-04 (compound 1a, Chapter 4) under the same conditions as 1. Unexpectedly, not only cathepsin labeling was found

Fusion of an activity based cysteine protease probe to the nonaarginine cell penetrating peptide would yield a probe that enters the cell in the fashion dictated by the

In Chapter 3, the two-step labeling approach presented in Chapter 2 was used to assess the specificity of two subunit-specific cell permeable inhibitors of the caspase-like

Deze probes binden covalent aan het te onderzoeken eiwit en zijn bovendien voorzien van een bio-orthogonale groep die inert is in de cellulaire omgeving, maar na cellysis