Biophysical and Biochemical Characterization of Nascent Polypeptide-Associated Complex of and Elucidation of Its Interacting Partners

Nascent polypeptide-associated complex (NAC) is a ribosome-associated molecular chaperone which is present only in archaea and eukaryotes. The primary function of NAC is to shield the newly synthesized polypeptide chains from inappropriate interactions with the cytosolic factors. Besides that, NAC has been implicated in diverse biological functions, which suggest that it might be a multifunctional protein. An elaborate study on NAC can provide useful information on protein folding in extreme conditions in which many archaea grow. Thus, in the present study, we have studied the biophysical and the biochemical characteristics of NAC of , an extreme thermoacidophilic archaeon. The study of protein-protein interactions and binding partners of a protein provides useful insights into the new/unreported roles of a protein. Thus, in this study, we have identified the binding partners of NAC in . The NAC protein of was cloned, expressed, and purified, and its binding partners were isolated by a pull down assay followed by identification with liquid chromatography-mass spectrometry. To the best of our knowledge, this is the first report on the biophysical and the biochemical characterization of NAC from and the identification of its interacting partners.