New technique speeds up production of protein nano-armor
Carnegie Mellon University researchers have developed methods that speed up the process of developing chemically linked synthetic and biological molecules by more than 10 times in natural conditions. The findings, which marry biology and chemistry, could make the production of bioconjugates for use in biomedicine, materials science, and other fields more efficient and cost effective.
Bioconjugates are formed when a biological molecule is joined with another molecule using covalent bonds. For example, in the case of biologic drugs, like interferon, the drug is connected to polymers that act like a cloak of nano-armor that protects the drug from damage until it reaches its target.
While promising, making bioconjugates has been expensive, time consuming and difficult to control.
Alan Russell, the Highmark Distinguished Career Professor, a professor of chemical engineering, and director of Carnegie Mellon's Disruptive Health Technology Institute, and Krzysztof Matyjaszewski, the J.C. Warner University Professor of Natural Science and a professor of chemistry, have discovered how to speed up the process and perform the chemistry of this process in truly natural conditions. Russell and Matyjaszewski co-direct the Center for Polymer-Based Protein Engineering at Carnegie Mellon.
Bioconjugates are traditionally made in solution, and purification after each step can take days or weeks. Even in the hands of a skilled scientist, it can take a week to make a few conjugates.
Russell and Matyjaszewski redesigned the chemistry for making bioconjugates to significantly decrease synthesis and purification time and made the approach so straightforward that even non-experts could create bioconjugates. The work—performed by a Carnegie Mellon team with Russell, Matyjaszewski, doctoral student Stefanie Baker, and researchers Hironobu Murata and Sheiliza Carmali—builds on a technique called Atom Transfer Radical Polymerization (ATRP), a novel method of polymer synthesis developed by Matyjaszewski's lab that has revolutionized the way macromolecules are made.
In a paper published in Nature Communications, they introduced the new method of growing polymers on proteins, known as Protein-ATRP on Reversible Immobilization Support (PARIS). It uses a "grafting-from" technique that exquisitely controls the growth of synthetic molecular hairs from the surface of proteins. These hairs can form a strong nano-armor that protects the biomolecule.
Russell and Matyjaszewski also recently published a major advance in creating bioconjugates using ATRP in Angewandte Chemie International Edition. ATRP is highly sensitive to atmospheric oxygen, which limits its use in natural conditions. This paper, co-authored by postdoctoral associate Alan Enciso and doctoral student Liye Fu, outlines a new method, known as "breathing ATRP," that is completely oxygen-tolerant.
"The basic idea was inspired by classical respiration cycles operating in cells," says Matyjaszewski, in an article for Nature Reviews Chemistry. "This is the first example of a fully oxygen-tolerant, well-controlled ATRP."
These new methods of growing polymers and armoring proteins have the potential to affect many aspects of our daily lives.
"Many people use enzymes in their everyday life," says Russell. "We use proteins and enzymes in laundry detergents, beer manufacturing, paper manufacturing, medicines, and so much more. Our work is aimed at improving the impact these proteins make on all our lives."
The research published in Nature Communications was funded by Carnegie Mellon University Center for Polymer-Based Protein Engineering.
The research published in Angewandte Chemie was funded by the National Science Foundation (1707490), the Mexican Council for Science and Technology and Carnegie Mellon University Center for Polymer-Based Protein Engineering.
Alan E. Enciso et al. A Breathing Atom-Transfer Radical Polymerization: Fully Oxygen-Tolerant Polymerization Inspired by Aerobic Respiration of Cells, Angewandte Chemie International Edition (2017). DOI: 10.1002/anie.201711105