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Direct polymerization of proteins. | LitMetric

Direct polymerization of proteins.

ACS Synth Biol

Department of Chemical Engineering, Stanford University, 381 North-South Mall, Stanford, California 94305, United States.

Published: June 2014

AI Article Synopsis

  • Researchers developed a one-step method to create active polymers of superfolder green fluorescent protein (sfGFP) using Click chemistry.
  • They inserted non-natural amino acids into sfGFP through cell-free protein synthesis, leading to the formation of linear or branched protein polymers that retained significant fluorescence activity.
  • This innovative approach allows for the synthesis of various protein polymers and biomaterials, with precise control over conjugation sites through genetic manipulation.

Article Abstract

We report the synthesis of active polymers of superfolder green fluorescent protein (sfGFP) in one step using Click chemistry. Up to six copies of the non-natural amino acids (nnAAs) p-azido-l-phenylalanine (pAzF) or p-propargyloxy-l-phenylalanine (pPaF) were site-specifically inserted into sfGFP by cell-free protein synthesis (CFPS). sfGFP containing two or three copies of these nnAAs were coupled by copper-catalyzed azide-alkyne cycloaddition to synthesize linear or branched protein polymers, respectively. The protein polymers retained ≥63% of their specific activity (i.e., fluorescence) after coupling. Polymerization of a concentrated solution of triply substituted sfGFP resulted in fluorescent macromolecular particles. Our method can be generalized to synthesize polymers of a protein or copolymers of any two or more proteins, and the conjugation sites can be determined exactly by standard genetic manipulation. Polymers of proteins and small molecules can also be created with this technology to make a new class of scaffolds or biomaterials.

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Source
http://dx.doi.org/10.1021/sb400116xDOI Listing

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