Improving Protein Expression, Stability, and Function with ProteinMPNN

Kiera H. Sumida(University of Washington), Reyes Núñez‐Franco(CIC bioGUNE), Indrek Kalvet(Howard Hughes Medical Institute), Samuel J. Pellock(University of Washington), Basile I. M. Wicky(University of Washington), Lukas F. Milles(University of Washington), Justas Dauparas(University of Washington), Jue Wang(University of Washington), Yakov Kipnis(Howard Hughes Medical Institute), Noel Jameson(University of Washington), Alex Kang(University of Washington), Joshmyn De La Cruz(University of Washington), Banumathi Sankaran(Lawrence Berkeley National Laboratory), Asim K. Bera(University of Washington), Gonzalo Jiménez‐Osés(Ikerbasque), David Baker(Howard Hughes Medical Institute)
Journal of the American Chemical Society
January 9, 2024
Cited by 289Open Access
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Abstract

Natural proteins are highly optimized for function but are often difficult to produce at a scale suitable for biotechnological applications due to poor expression in heterologous systems, limited solubility, and sensitivity to temperature. Thus, a general method that improves the physical properties of native proteins while maintaining function could have wide utility for protein-based technologies. Here, we show that the deep neural network ProteinMPNN, together with evolutionary and structural information, provides a route to increasing protein expression, stability, and function. For both myoglobin and tobacco etch virus (TEV) protease, we generated designs with improved expression, elevated melting temperatures, and improved function. For TEV protease, we identified multiple designs with improved catalytic activity as compared to the parent sequence and previously reported TEV variants. Our approach should be broadly useful for improving the expression, stability, and function of biotechnologically important proteins.


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