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G.V.T. Swapna

Rutgers, The State University of New Jersey

ORCID: 0000-0001-9342-2525

Publishes on Protein Structure and Dynamics, RNA and protein synthesis mechanisms, Enzyme Structure and Function. 203 papers and 3k citations.

203Publications
3kTotal Citations

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Top publicationsby citations

Structure of Antibacterial Peptide Microcin J25:  A 21-Residue Lariat Protoknot
Marvin J. Bayro, Jayanta Mukhopadhyay, G.V.T. Swapna et al.|Journal of the American Chemical Society|2003
Cited by 206

The antibacterial peptide microcin J25 (MccJ25) inhibits bacterial transcription by binding within, and obstructing, the nucleotide-uptake channel of bacterial RNA polymerase. Published covalent and three-dimensional structures indicate that MccJ25 is a 21-residue cycle. Here, we show that the published covalent and three-dimensional structures are incorrect, and that MccJ25 in fact is a 21-residue "lariat protoknot", consisting of an 8-residue cyclic segment followed by a 13-residue linear segment that loops back and threads through the cyclic segment. MccJ25 is the first example of a lariat protoknot involving a backbone-side chain amide linkage.

A microscale protein NMR sample screening pipeline
Paolo Rossi, G.V.T. Swapna, Yuanpeng J. Huang et al.|Journal of Biomolecular NMR|2009
Cited by 139Open Access

As part of efforts to develop improved methods for NMR protein sample preparation and structure determination, the Northeast Structural Genomics Consortium (NESG) has implemented an NMR screening pipeline for protein target selection, construct optimization, and buffer optimization, incorporating efficient microscale NMR screening of proteins using a micro-cryoprobe. The process is feasible because the newest generation probe requires only small amounts of protein, typically 30-200 microg in 8-35 microl volume. Extensive automation has been made possible by the combination of database tools, mechanization of key process steps, and the use of a micro-cryoprobe that gives excellent data while requiring little optimization and manual setup. In this perspective, we describe the overall process used by the NESG for screening NMR samples as part of a sample optimization process, assessing optimal construct design and solution conditions, as well as for determining protein rotational correlation times in order to assess protein oligomerization states. Database infrastructure has been developed to allow for flexible implementation of new screening protocols and harvesting of the resulting output. The NESG micro NMR screening pipeline has also been used for detergent screening of membrane proteins. Descriptions of the individual steps in the NESG NMR sample design, production, and screening pipeline are presented in the format of a standard operating procedure.