Methods for Expression of Recombinant Proteins Using a Pichia pastoris Cell-Free System

Abstract

Cell-free protein synthesis is a powerful tool for engineering biology and has been utilized in many diverse applications, from biosensing and protein prototyping to biomanufacturing and the design of metabolic pathways. By exploiting host cellular machinery decoupled from cellular growth, proteins can be produced in vitro both on demand and rapidly. Eukaryotic cell-free platforms are often neglected due to perceived complexity and low yields relative to their prokaryotic counterparts, despite providing a number of advantageous properties. The yeast Pichia pastoris (also known as Komagataella phaffii) is a particularly attractive eukaryotic host from which to generate cell-free extracts, due to its ability to grow to high cell densities with high volumetric productivity, genetic tractability for strain engineering, and ability to perform post-translational modifications. Here, we describe methods for conducting cell-free protein synthesis using P. pastoris as the host, from preparing the cell lysates to protocols for both coupled and linked transcription-translation reactions. By providing these methodologies, we hope to encourage the adoption of the platform by new and experienced users alike. © 2020 The Authors.

Basic Protocol 1: Preparation of Pichia pastoris cell lysate

Basic Protocol 2: Coupled in vitro transcription and translation

Basic Protocol 3: Determining luciferase production from cell-free protein synthesis reactions

Alternate Protocol 1: Linked in vitro transcription and translation

Alternate Protocol 2: Quantifying HSA protein concentration

Support Protocol 1: Preparation of mRNA by in vitro transcription for linked transcription and translation