The Center for Gene Regulation in Health and Disease (GRHD), Cleveland State University, Cleveland, OH.
Professor Anton A Komar received both his undergraduate and graduate degrees from the Department of Molecular Biology at Moscow State University (Moscow, Russia), 1985 and 1991 respectively. Thereafter he worked in several European countries on various aspects of protein biosynthesis and folding. In 2001 he moved to Cleveland State University, Ohio, USA where he since 2014 is Director of the Centre for Gene Regulation in Health and Disease.
For any protein to function properly, the polypeptide chain produced by the ribosome has to fold into a correct three-dimensional structure. Protein folding in vivo begins co-translationally when the nascent peptide emerges from the ribosome exit tunnel. We and others suggested that choice of synonymous codons in mRNA may alter the properties of a protein; however, the mechanisms behind such effects remained unclear. Here we show how the use of different synonymous codons results in a change of local and global translational kinetics, altering the pathway of co-translational folding, as well as the ultimate stable conformation attained by a model protein, mammalian eye lens gamma-B crystallin, as assessed by 2D-NMR. We investigate translation and co-translational folding in a time-resolved manner, providing evidence that the structural difference between synonymous variants arise at the level of co-translational folding. Our study provides important insights into the mechanism of protein folding in the cell and contributes to better understanding of the relationship between degeneracy of the genetic code, genotype and phenotype, origin of human diseases caused by synonymous mutations leading to incorrect protein folding and gives a tool to upscale and evaluate the production of functional proteins for medical and biotechnological purposes. These studies in particular led to a start-up biotech company DAPCEL, Inc.
Komar AA. The yin and yang of codon usage. Hum Mol Genet., 2016.
Buhr et al, Synonymous codons direct cotranslational folding toward different protein conformations. Mol. Cell, 2016.
Holtkamp et al, Cotranslational protein folding on the ribosome monitored in real time. Science, 2015
Komar AA. A pause for thought along the co-translational folding pathway. Trends Biochem Sci. 2009.
Host: Suparna Sanyal
Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information.
Any cookies that may not be particularly necessary for the website to function and is used specifically to collect user personal data via analytics, ads, other embedded contents are termed as non-necessary cookies. It is mandatory to procure user consent prior to running these cookies on your website.