Synthesis of Cyclopropene‐Modified Fatty Acids Allows Single‐Cell Quantification of Uptake by Immune Cells

L Luuk Reinalda (Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands) G Graham A. Heieis (Department of Parasitology Leiden University Medical Center Leiden the Netherlands) L Laura Bogue Edgerton (Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands) K Kristine Bertheussen (Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands) D Diana Torres‐García (Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands) M Marouane el Boujadayni (Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands) K Kas Steuten J Jeroen M. Punt (Department of Molecular Physiology Leiden University Leiden the Netherlands) W Wouter P. F. Driever (Department of Molecular Physiology Leiden University Leiden the Netherlands) C Connor Corrigan (School of Biochemistry and Immunology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland) X Xinyuan Wang B Bart Everts (Department of Parasitology Leiden University Medical Center Leiden the Netherlands) D David Finlay (School of Biochemistry and Immunology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland) M Mario van der Stelt (Division of Drug Discovery and Safety, Leiden Academic Centre for Drug Research) S Sander I. van Kasteren

Abstract

ABSTRACT Immune cell activity is strongly influenced by the nutrients present during activation. The effects of specific fatty acids (FAs) can be particularly complex, with them exerting diverse and sometimes opposing effects on immune cells. These functional differences are thought to stem from structural differences between the FAs, leading to altered cellular handling. However, chemical tools to directly probe these aspects remain limited. Here, we report the design and synthesis of saturated, unsaturated, and polyunsaturated cyclopropenyl fatty acids, each incorporating a minimal one‐carbon cyclopropene moiety as a bioorthogonal click handle. This motif enables rapid and live‐cell‐compatible labeling via the inverse electron‐demand Diels–Alder reaction, providing a versatile platform to trace FA behavior in biological systems. Application of these synthetic cyclopropenyl FAs in primary immune cell mixtures reveals distinct uptake patterns between different cell types, with polyunsaturated analogues showing strong uptake across all immune cell types. Complementary metabolic and proteomic analyses suggest that this uptake results in biological differences between high/low uptake immune populations, highlighting the utility of cyclopropenyl FA probes for dissecting lipid uptake in the context of immune cell biology.

Article Details

Volume / Issue Vol. 65, Issue 31
Published July 27, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (15)

L

Luuk Reinalda

Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands

G

Graham A. Heieis

Department of Parasitology Leiden University Medical Center Leiden the Netherlands

L

Laura Bogue Edgerton

Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands

K

Kristine Bertheussen

Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands

D

Diana Torres‐García

Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands

M

Marouane el Boujadayni

Division of Chemical Biology and Immunology Leiden Institute of Chemistry and the Institute for Chemical Immunology Leiden University Leiden the Netherlands

K

Kas Steuten

J

Jeroen M. Punt

Department of Molecular Physiology Leiden University Leiden the Netherlands

W

Wouter P. F. Driever

Department of Molecular Physiology Leiden University Leiden the Netherlands

C

Connor Corrigan

School of Biochemistry and Immunology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland

X

Xinyuan Wang

B

Bart Everts

Department of Parasitology Leiden University Medical Center Leiden the Netherlands

D

David Finlay

School of Biochemistry and Immunology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland

M

Mario van der Stelt

Division of Drug Discovery and Safety, Leiden Academic Centre for Drug Research

S

Sander I. van Kasteren