Structural biology of Gram-positive bacterial adhesins

被引:81
|
作者
Vengadesan, Krishnan
Narayana, Sthanam V. L. [1 ]
机构
[1] Univ Alabama Birmingham, Ctr Biophys Sci & Engn, Birmingham, AL 35294 USA
关键词
bacterial adhesions; Gram-positive pili; pilins; protein structure; FIBRONECTIN-BINDING-PROTEINS; STAPHYLOCOCCUS-AUREUS; CRYSTAL-STRUCTURE; CORYNEBACTERIUM-DIPHTHERIAE; STREPTOCOCCUS-AGALACTIAE; LIGAND-BINDING; STABILIZING ISOPEPTIDE; IMMUNOGLOBULIN FOLD; HUMAN-FIBRINOGEN; SURFACE PROTEIN;
D O I
10.1002/pro.613
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structural biology of Gram-positive cell surface adhesins is an emerging field of research, whereas Gram-negative pilus assembly and anchoring have been extensively investigated and are well understood. Gram-positive surface proteins known as MSCRAMMs (microbial surface components recognizing adhesive matrix molecules) and individual proteins that assemble into long, hair-like organelles known as pili have similar features at the primary sequence level as well as at the tertiary structural level. Some of these conserved features are essential for their transportation from the cytoplasm and for cell wall anchoring. More importantly, the MSCRAMMs and the individual pilins are assembled with building blocks that are variants of structural modules used for human immunoglobulins. MSCRAMMs target the host's extracellular matrix proteins, such as collagen, fibrinogen, and fibronectin, and they have received considerable attention from structural biologists in the last decade, who have primarily been interested in understanding their interactions with host tissue. The recent focus is on the newly discovered pili of Gram-positive bacteria, and in this review, we highlight the advances in understanding of the individual pilus constituents and their associations and stress the similarities between the individual pilins and surface proteins.
引用
收藏
页码:759 / 772
页数:14
相关论文
共 50 条
  • [21] Gram-positive bacterial conjugation: new structural insight on plasmid pIP501
    Goessweiner-Mohr, N.
    Fercher, C.
    Celik, E. -K.
    Arends, K.
    Grohmann, E.
    Keller, W.
    ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2011, 67 : C738 - C739
  • [22] Structural basis of Synercid® (quinupristin-dalfopristin) resistance in gram-positive bacterial pathogens
    Kehoe, LE
    Snidwongse, J
    Courvalin, P
    Rafferty, JB
    Murray, IA
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) : 29963 - 29970
  • [23] Anchorless adhesins and invasins of Gram-positive bacteria: A new class of virulence factors - Response
    Jenkinson, HF
    TRENDS IN MICROBIOLOGY, 2002, 10 (05) : 208 - 208
  • [24] GRAM-POSITIVE
    不详
    LANCET, 1946, 250 (JAN12): : 61 - 61
  • [25] GRAM-POSITIVE
    AINLEYWALKER, EW
    LANCET, 1946, 250 (JAN19): : 110 - 110
  • [26] Metabolism of the Gram-Positive Bacterial Pathogen Listeria monocytogenes
    Sauer, John-Demian
    Herskovits, Anat A.
    O'Riordan, Mary X. D.
    MICROBIOLOGY SPECTRUM, 2019, 7 (04):
  • [27] Gram-positive bacterial resistance - A challenge for the next millennium
    Bassetti, M
    Melica, G
    Cenderello, G
    Rosso, R
    Di Biagio, A
    Bassetti, D
    PANMINERVA MEDICA, 2002, 44 (03) : 179 - 184
  • [28] Strategies for the successful treatment of gram-positive bacterial infections
    Remington, JS
    CLINICAL INFECTIOUS DISEASES, 2000, 31 : S150 - S151
  • [29] An Increase of Gram-Positive Bacteria in Spontaneous Bacterial Peritonitis
    Nookala, Vinod K.
    Sharzehi, Kaveh
    Lee, Tai-Ping
    GASTROENTEROLOGY, 2012, 142 (05) : S951 - S951
  • [30] Novel antibiotics for the treatment of gram-positive bacterial infections
    Brands, M
    Endermann, R
    Gahlmann, R
    Krüger, J
    Raddatz, S
    Stoltefuss, J
    Belov, VN
    Nizamov, S
    Sokolov, VV
    de Meijere, A
    JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (19) : 4246 - 4253