Diagram of a new approach to electrochemical protein labelling strategies.

精东影业 research team sparks a new catalytic process

Team used a mild charge of electricity to precisely modify proteins鈥攚ork that could have implications for targeting cancer cells

Boston College researchers have used a mild charge of electricity to precisely modify proteins鈥攁 new and inexpensive tool that can be used to develop novel biotherapeutics and protein-based research tools.

Led by Chemistry Professors Abhishek Chatterjee and Eranthie Weerapana, the team developed and optimized a novel electrochemical protein labeling reaction called "eCLIC", that enables precise modification of site-specifically incorporated 5-hydroxytryptophan (5HTP) residues on many different proteins including full-length therapeutic antibodies.听

Abhishek Chatterjee

Abhishek Chatterjee (Lee Pellegrini)

鈥淲e used this strategy to generate many site-specific protein conjugates, including an antibody-cytotoxic drug conjugate that selectively enters and kills cancer cells, but not non-cancer cells,鈥 said Chatterjee. 鈥淎 key advantage of eCLIC is the reagents needed for this method are really inexpensive, costing less than $10 a gram.鈥

The team鈥檚 success marked the first time electrocatalysis has been used to achieve protein modification in a site-specific manner, they reported in an article published in the journal听Nature Chemistry, 鈥淓lectrochemical labeling of hydroxyindoles with chemoselectivity for site-specific protein bioconjugation.鈥

Proteins are large molecules, typically composed of hundreds of amino acid monomers, Chatterjee noted. The ability to selectively modify proteins at predefined sites is important for many applications. For example, by covalently attaching toxic drugs to antibodies, it has been possible to selectively deliver them to cancer cells, resulting in both improved therapeutic efficacy and reduced off-target toxicity.

Many research applications also require the attachment of biophysical probes onto various proteins. The ability to define the site of modification on proteins is critical to ensure that important protein functions are not harmed, Chatterjee said.

鈥淭he challenge arises from the fact that all proteins are made from 20 amino acids in various combinations,鈥 he said. 鈥淚dentifying a modifiable functionality at the desired site, not repeated elsewhere, is typically challenging, which makes it difficult to achieve site-specificity in protein modification.鈥

Eranthie Weerapana

Eranthie Weerapana (Lee Pellegrini)

To overcome these challenges, the team sought to develop a method to incorporate a non-natural amino acid at any chosen site or sites of a protein. The team accomplished this by reengineering the translation system of cells to accommodate the new amino acid 5HTP.

In addition, the researchers wanted to design chemical reactions that could be used to selectively modify this nonnatural amino acid in the presence of all of the natural amino acids, Chatterjee said.

鈥淚f we could do this, we could provide a general method to generate proteins with a built-in 'attachment-handle' at a predefined site. In particular, we were interested in developing a reaction that would use electricity to catalyze the protein modification reaction, instead of chemical catalysis, since the former is inexpensive, environmentally friendly, and gentle on delicate proteins.鈥

Chatterjee said the team was able to overcome an unusual challenge when they first tried to model the reaction. Typically, researchers start with small molecules, in this case 5HTP and aniline, then move on to large proteins.

But first attempts at the reaction between 5HTP and anilines at the small-molecule level were messy, as the 5HTP molecules reacted preferentially with each other. When 5HTP was incorporated into a large protein, however, it was no longer able to react with another protein-bound 5HTP, and cleanly reacted with an aniline instead, the team reported.

鈥淚f we had stuck with the traditional progression鈥攆rom small to large鈥攚e'd have never pursued eCLIC, thinking 鈥業t's too messy,鈥欌 Chatterjee said. 鈥淚nstead, we did our reaction development non-traditionally, directly on a protein, which helped us realize how clean and selective it was in this setting.鈥

To further advance the eCLIC strategy for large-scale modification of important protein targets, this technology has been licensed toBrickBio Inc., which Chatterjee co-founded. Future research will focus on developing next-generation, site-specifically modified protein-based biotherapeutics and research reagents.

In addition to Chatterjee and Weerapana, co-authors of the paper were post-doctoral researchers Soumya Jyoti, Atanu Mondal, and Singha Roy; and graduate students Conor Loynd, Vincent J. Ovalle, Sarah E. Canarelli, Delilah Jewel, and Elise D. Ficaretta.