In organello protein synthesis.

Abstract

Protein synthesis by isolated plant mitochondria under in vitro conditions is a direct method to study the translational products of this organellar genetic system. Compared to fungal and animal mitochondrial systems, a considerably higher number of proteins is expected to be encoded by the plant mitochondrial genome (for details, see the introduction to Chapter 32). Since no in vitro translation system using isolated mitochondrial ribosomes, e.g., in an S100 extract, has yet been established, protein synthesis with intact organelles is the best way to analyze the products of the mitochondrial translation apparatus. The in organello synthesized proteins should in fact reflect the number of polypeptides expressed by plant mitochondria. The analysis relies on incubation of isolated mitochondria with radiolabeled amino acids such as [35S]methionine. After a period of continuing the in organello synthesis the radiolabeled translation products are subsequently separated by SDS polyacrylamide gel electrophoresis and analyzed by autoradiography (Fig. 1). Such an experimental procedure was developed and has been described in detail by Leaver et al. (). The system established by these authors has reproducibly worked well with mitochondria from different tissues of various plants and here we describe this method with minor changes. Open image in new window Fig. 1. Autoradiograph of in organello [35S]labeled translation products from plant mitochondria separated on a 15% SDS-polyacrylamide gel. Lane (1), total translation products of potato mitochondria were directly loaded on the gel. Lane (2), after incubation with an antibody directed against the overexpressed wheat mitochondrial NAD9 protein and subsequent immunoprecipitation with Protein-A Sepharose. Assignments of individual labeled bands are given on the left side and the molecular mass standards are on the right hand margin.