Identification of Chlamydia trachomatis Outer Membrane Complex Proteins by Differential Proteomics

被引:63
作者
Liu, Xiaoyun [2 ]
Afrane, Mary [1 ]
Clemmer, David E. [2 ]
Zhong, Guangming [3 ]
Nelson, David E. [1 ]
机构
[1] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
[2] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Microbiol & Immunol, San Antonio, TX 78229 USA
关键词
PEPTIDOGLYCAN-ASSOCIATED LIPOPROTEIN; ENVELOPE PROTEINS; GENOME SEQUENCE; IN-VITRO; PSITTACI; AUTOTRANSPORTER; PATHOGEN; ANTIGEN; SURFACE; FAMILY;
D O I
10.1128/JB.01628-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The extracellular chlamydial infectious particle, or elementary body (EB), is enveloped by an intra-and intermolecular cysteine cross-linked protein shell called the chlamydial outer membrane complex (COMC). A few abundant proteins, including the major outer membrane protein and cysteine-rich proteins (OmcA and OmcB), constitute the overwhelming majority of COMC proteins. The identification of less-abundant COMC proteins has been complicated by limitations of proteomic methodologies and the contamination of COMC fractions with abundant EB proteins. Here, we used parallel liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) analyses of Chlamydia trachomatis serovar L2 434/Bu EB, COMC, and Sarkosyl-soluble EB fractions to identify proteins enriched or depleted from COMC. All well-described COMC proteins were specifically enriched in the COMC fraction. In contrast, multiple COMC-associated proteins found in previous studies were strongly enriched in the Sarkosyl-soluble fraction, suggesting that these proteins are not COMC components or are not stably associated with COMC. Importantly, we also identified novel proteins enriched in COMC. The list of COMC proteins identified in this study has provided reliable information for further understanding chlamydial protein secretion systems and modeling COMC and EB structures.
引用
收藏
页码:2852 / 2860
页数:9
相关论文
共 70 条
[41]  
Longbottom D, 1996, FEMS MICROBIOL LETT, V142, P277
[42]   In vitro and in vivo functional activity of Chlamydia MurA, a UDP-N-acetylglucosamine enolpyruvyl transferase involved in peptidoglycan synthesis and fosfomycin resistance [J].
McCoy, AJ ;
Sandlin, RC ;
Maurelli, AT .
JOURNAL OF BACTERIOLOGY, 2003, 185 (04) :1218-1228
[43]   Building the invisible wall: updating the chlamydial peptidoglycan anomaly [J].
McCoy, AJ ;
Maurelli, AT .
TRENDS IN MICROBIOLOGY, 2006, 14 (02) :70-77
[44]   Characterization of Chlamydia MurC-Ddl, a fusion protein exhibiting D-alanyl-D-alanine ligase activity involved in peptidoglycan synthesis and D-cycloserine sensitivity [J].
McCoy, AJ ;
Maurelli, AT .
MOLECULAR MICROBIOLOGY, 2005, 57 (01) :41-52
[45]   L,L-diaminopimelate aminotransferase, a trans-kingdom enzyme shared by Chlamydia and plants for synthesis of diaminopimelate/lysine [J].
McCoy, Andrea J. ;
Adams, Nancy E. ;
Hudson, Andre O. ;
Gilvarg, Charles ;
Leustek, Thomas ;
Maurelli, Anthony T. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (47) :17909-17914
[46]   ISOLATION AND CHARACTERIZATION OF A GENE ENCODING A CHLAMYDIA-PNEUMONIAE 76-KILODALTON PROTEIN CONTAINING A SPECIES-SPECIFIC EPITOPE [J].
MELGOSA, MP ;
KUO, CC ;
CAMPBELL, LA .
INFECTION AND IMMUNITY, 1994, 62 (03) :880-886
[47]   The Chlamydia outer membrane protein OmcB is required for adhesion and exhibits biovar-specific differences in glycosaminoglycan binding [J].
Moelleken, Katja ;
Hegemann, Johannes H. .
MOLECULAR MICROBIOLOGY, 2008, 67 (02) :403-419
[48]   CHLAMYDIAL DISEASE PATHOGENESIS - THE 57-KD CHLAMYDIAL HYPERSENSITIVITY ANTIGEN IS A STRESS RESPONSE PROTEIN [J].
MORRISON, RP ;
BELLAND, RJ ;
LYNG, K ;
CALDWELL, HD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (04) :1271-1283
[49]   Immunity to murine chlamydial genital infection [J].
Morrison, RP ;
Caldwell, HD .
INFECTION AND IMMUNITY, 2002, 70 (06) :2741-2751
[50]   INTERACTION OF CHLAMYDIAE AND HOST-CELLS INVITRO [J].
MOULDER, JW .
MICROBIOLOGICAL REVIEWS, 1991, 55 (01) :143-190