Nature-inspired protein ligation and its applications

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作者
Rasmus Pihl
Qingfei Zheng
Yael David
机构
[1] Memorial Sloan Kettering Cancer Center,Chemical Biology Program
[2] Aarhus University,Department of Biomedicine
[3] The Ohio State University,Department of Radiation Oncology, College of Medicine
[4] The Ohio State University,Center for Cancer Metabolism, James Comprehensive Cancer Center
[5] The Ohio State University,Department of Biological Chemistry and Pharmacology, College of Medicine
[6] Weill Cornell Medicine,Department of Pharmacology
[7] Weill Cornell Medicine,Department of Physiology, Biophysics and Systems Biology
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The ability to manipulate the chemical composition of proteins and peptides has been central to the development of improved polypeptide-based therapeutics and has enabled researchers to address fundamental biological questions that would otherwise be out of reach. Protein ligation, in which two or more polypeptides are covalently linked, is a powerful strategy for generating semisynthetic products and for controlling polypeptide topology. However, specialized tools are required to efficiently forge a peptide bond in a chemoselective manner with fast kinetics and high yield. Fortunately, nature has addressed this challenge by evolving enzymatic mechanisms that can join polypeptides using a diverse set of chemical reactions. Here, we summarize how such nature-inspired protein ligation strategies have been repurposed as chemical biology tools that afford enhanced control over polypeptide composition.
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页码:234 / 255
页数:21
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