Acrolein as an Alternative Broadly Reactive Activity-Based Probe for Activity-Based Protein Profiling of Cysteinome

Iodoacetamide (IAM)-based probes have established the activity-based protein profiling (ABPP) paradigm; however, their reliance on the SN2 mechanism limits the labeling of all cysteine residues, highlighting the need for complementary probes based on alternative reactions. Additionally, probe design must balance between minimizing probe size and simplifying workflow complexity. As a solution to the above issues, we propose acrolein (ACR), a simple α, β-unsaturated carbonyl compound, as an alternative broadly reactive ABPP probe. ACR possesses sp<sup>2</sup>-hybridized electrophilic groups that react with nucleophilic amino acids via Michael addition, and its aldehyde group facilitates efficient enrichment. We developed a user-friendly chemoproteomic platform for ACR, enabling the identification of over 28,000 nucleophilic residues across three cell lines. ACR demonstrated its ability to detect reactivity changes in nucleophilic residues under native and denatured conditions and to identify known targets of entacapone. Overall, ACR represents a versatile and efficient tool for studying functional nucleophilic sites, with potential applications in drug discovery.

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Publication Details

Journal
Analytical Chemistry
Published
2025-07-16
DOI
https://doi.org/10.1021/acs.analchem.5c00022
Primary Topic
Click Chemistry and Applications
Type
article
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article

Acrolein as an Alternative Broadly Reactive Activity-Based Probe for Activity-Based Protein Profiling of Cysteinome

Kailu Tian, Mingliang Ye, Hongqiang Qin, Chengfei Ruan et al.
Analytical Chemistry
Click Chemistry and Applications
article

Acrolein as an Alternative Broadly Reactive Activity-Based Probe for Activity-Based Protein Profiling of Cysteinome

Kailu Tian, Mingliang Ye, Hongqiang Qin, Chengfei Ruan, Xiang‐Xin Zhang, Jiaying Li, Jiahua Zhou, Yan Wang, Yanan Li
article en

Abstract

Iodoacetamide (IAM)-based probes have established the activity-based protein profiling (ABPP) paradigm; however, their reliance on the SN2 mechanism limits the labeling of all cysteine residues, highlighting the need for complementary probes based on alternative reactions. Additionally, probe design must balance between minimizing probe size and simplifying workflow complexity. As a solution to the above issues, we propose acrolein (ACR), a simple α, β-unsaturated carbonyl compound, as an alternative broadly reactive ABPP probe. ACR possesses sp<sup>2</sup>-hybridized electrophilic groups that react with nucleophilic amino acids via Michael addition, and its aldehyde group facilitates efficient enrichment. We developed a user-friendly chemoproteomic platform for ACR, enabling the identification of over 28,000 nucleophilic residues across three cell lines. ACR demonstrated its ability to detect reactivity changes in nucleophilic residues under native and denatured conditions and to identify known targets of entacapone. Overall, ACR represents a versatile and efficient tool for studying functional nucleophilic sites, with potential applications in drug discovery.

Analytical ChemistryVol. 97(29)
Dalian Institute of Chemical Physics (CN), Chinese Academy of Sciences (CN), Dalian University of Technology (CN), Beijing Proteome Research Center (CN), State Key Laboratory of Chemical Engineering (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 87%
Click Chemistry and Applications
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