Using Modern Tools To Probe the Structure–Function Relationship of Fatty Acid Synthases |
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| Authors: | Kara Finzel D. John Lee Prof. Michael D. Burkart |
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| Affiliation: | Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA 92093‐0358 (USA) |
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| Abstract: | Fatty acid biosynthesis is essential to life and represents one of the most conserved pathways in nature, preserving the same handful of chemical reactions across all species. Recent interest in the molecular details of the de novo fatty acid synthase (FAS) has been heightened by demand for renewable fuels and the emergence of multidrug‐resistant bacterial strains. Central to FAS is the acyl carrier protein (ACP), a protein chaperone that shuttles the growing acyl chain between catalytic enzymes within the FAS. Human efforts to alter fatty acid biosynthesis for oil production, chemical feedstock, or antimicrobial purposes has been met with limited success, due in part to a lack of detailed molecular information behind the ACP–partner protein interactions inherent to the pathway. This review will focus on recently developed tools for the modification of ACP and analysis of protein–protein interactions, such as mechanism‐based crosslinking, and the studies exploiting them. Discussion specific to each enzymatic domain will focus first on mechanism and known inhibitors, followed by available structures and known interactions with ACP. Although significant unknowns remain, new understandings of the intricacies of FAS point to future advances in manipulating this complex molecular factory. |
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| Keywords: | acyl carrier protein biosynthesis crosslinkers fatty acids inhibitors |
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