TMB Finding Pipeline: Novel Approach for Detecting β-Barrel Membrane Proteins in Genomic Sequences

We have developed a novel approach for dissecting transmembrane beta-barrel proteins (TMBs) in genomic sequences. The features include (i) the identification of TMBs using the preference of residue pairs in globular, transmembrane helical (TMH) and TMBs, (ii) elimination of globular/TMH proteins that show sequence identity of more than 70% for the coverage of 80% residues with known structures, (iii) elimination of globular/TMH proteins that have sequence identity of more than 60% with known sequences in SWISS-PROT, and (iv) exclusion of TMH proteins using SOSUI, a prediction system for TMH proteins. Our approach picked up 7% TMBs in all the considered genomes. The comparison between the identified TMBs in E. coli genome and available experimental data demonstrated that the new approach could correctly identify all the 11 known TMBs, whose crystal structures are available. Further, it revealed the presence of 19 TMBs, homology with known structures, 60 TMBs similar to well annotated sequences, and 54 TMBs that have high sequence similarity with Escherichia coli beta-barrel proteins deposited in Transport Classification Database (TCDB). Interestingly, the present approach identified TMBs from all 15 families in TCDB. In human genome, the occurrence of TMBs varies from 0 to 3% in different chromosomes. We suggest that our approach could lead to a step forward in the advancement of structural and functional genomics.

[1]  J. Jenkins,et al.  The structure of OmpF porin in a tetragonal crystal form. , 1995, Structure.

[2]  Wing-Yiu Choy,et al.  Solution structure and dynamics of the outer membrane enzyme PagP by NMR , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[3]  Paul Horton,et al.  Discrimination of outer membrane proteins using support vector machines , 2005, Bioinform..

[4]  Andrew D. Ferguson,et al.  Crystal structure of the Outer Membrane Transporter FecA , 2002 .

[5]  P K Ponnuswamy,et al.  Identification of membrane spanning beta strands in bacterial porins. , 1997, Protein engineering.

[6]  G. Schulz,et al.  High-resolution structure of the OmpA membrane domain. , 2000, Journal of molecular biology.

[7]  M. Saier,et al.  The Transporter Classification (TC) System, 2002 , 2002, Critical reviews in biochemistry and molecular biology.

[8]  Shandar Ahmad,et al.  Application of residue distribution along the sequence for discriminating outer membrane proteins , 2005, Comput. Biol. Chem..

[9]  M. Saier,et al.  The β‐barrel finder (BBF) program, allowing identification of outer membrane β‐barrel proteins encoded within prokaryotic genomes , 2002 .

[10]  Rita Casadio,et al.  New Escherichia coli outer membrane proteins identified through prediction and experimental verification , 2006, Protein science : a publication of the Protein Society.

[11]  David R. Westhead,et al.  TMB-Hunt: a web server to screen sequence sets for transmembrane β-barrel proteins , 2005, Nucleic Acids Res..

[12]  Stavros J. Hamodrakas,et al.  Evaluation of methods for predicting the topology of β-barrel outer membrane proteins and a consensus prediction method , 2005, BMC Bioinformatics.

[13]  Henry R. Bigelow,et al.  Predicting transmembrane beta-barrels in proteomes. , 2004, Nucleic acids research.

[14]  Piero Fariselli,et al.  A sequence-profile-based HMM for predicting and discriminating beta barrel membrane proteins , 2002, ISMB.

[15]  S. Krishnaswamy,et al.  Profiles from structure based sequence alignment of porins can identify ß stranded integral membrane proteins , 2000, Bioinform..

[16]  Qi Liu,et al.  Identification of -barrel membrane proteins based on amino acid composition properties and predicted secondary structure , 2003, Comput. Biol. Chem..

[17]  T. N. Bhat,et al.  The Protein Data Bank , 2000, Nucleic Acids Res..

[18]  Ingvar Eidhammer,et al.  BOMP: a program to predict integral ?barrel outer membrane proteins encoded within genomes of Gram-negative bacteria , 2004, Nucleic Acids Res..

[19]  G. Rummel,et al.  Crystal structures explain functional properties of two E. coli porins , 1992, Nature.

[20]  Yukimitsu Yabuki,et al.  GENIUS II: a high-throughput database system for linking ORFs in complete genomes to known protein three-dimensional structures , 2004, Bioinform..

[21]  M Michael Gromiha,et al.  Motifs in outer membrane protein sequences: applications for discrimination. , 2005, Biophysical chemistry.

[22]  W. Wimley Toward genomic identification of β‐barrel membrane proteins: Composition and architecture of known structures , 2002, Protein science : a publication of the Protein Society.

[23]  Makiko Suwa,et al.  Automatic gene collection system for genome-scale overview of G-protein coupled receptors in eukaryotes. , 2005, Gene.

[24]  Harpreet Kaur,et al.  Prediction of transmembrane regions of beta-barrel proteins using ANN- and SVM-based methods. , 2004, Proteins.

[25]  Stavros J. Hamodrakas,et al.  A Hidden Markov Model method, capable of predicting and discriminating β-barrel outer membrane proteins , 2004, BMC Bioinformatics.

[26]  K. Diederichs,et al.  Siderophore-mediated iron transport: crystal structure of FhuA with bound lipopolysaccharide. , 1998, Science.

[27]  Ke Wang,et al.  PSORT-B: improving protein subcellular localization prediction for Gram-negative bacteria , 2003, Nucleic Acids Res..

[28]  J. Deisenhofer,et al.  Structural basis of gating by the outer membrane transporter FecA. , 2002, Science.

[29]  P. van Gelder,et al.  Structure and function of bacterial outer membrane proteins: barrels in a nutshell , 2000, Molecular microbiology.

[30]  Gunnar von Heijne,et al.  Experimentally constrained topology models for 51,208 bacterial inner membrane proteins. , 2005, Journal of molecular biology.

[31]  K. H. Kalk,et al.  Structural evidence for dimerization-regulated activation of an integral membrane phospholipase. , 1999 .

[32]  M. Michael Gromiha,et al.  A simple statistical method for discriminating outer membrane proteins with better accuracy , 2005, Bioinform..

[33]  P Gros,et al.  Crystal structure of the outer membrane protease OmpT from Escherichia coli suggests a novel catalytic site , 2001, The EMBO journal.

[34]  Shigeki Mitaku,et al.  SOSUI: classification and secondary structure prediction system for membrane proteins , 1998, Bioinform..

[35]  G. Schulz,et al.  The structure of the outer membrane protein OmpX from Escherichia coli reveals possible mechanisms of virulence. , 1999, Structure.