Multivalent glycoconjugates as anti-pathogenic agents

被引:439
作者
Bernardi, Anna [1 ,2 ]
Jimenez-Barbero, Jesus [3 ]
Casnati, Alessandro [4 ]
De Castro, Cristina [5 ]
Darbre, Tamis [6 ]
Fieschi, Franck [7 ]
Finne, Jukka [8 ]
Funken, Horst [9 ]
Jaeger, Karl-Erich [9 ]
Lahmann, Martina [10 ]
Lindhorst, Thisbe K. [11 ]
Marradi, Marco [12 ,13 ]
Messner, Paul [14 ]
Molinaro, Antonio [5 ]
Murphy, Paul V. [15 ]
Nativi, Cristina [16 ]
Oscarson, Stefan [17 ]
Penades, Soledad [12 ,13 ]
Peri, Francesco [18 ]
Pieters, Roland J. [19 ]
Renaudet, Olivier [20 ,21 ]
Reymond, Jean-Louis [6 ]
Richichi, Barbara [16 ]
Rojo, Javier [22 ]
Sansone, Francesco [4 ]
Schaeffer, Christina [14 ]
Turnbull, W. Bruce [23 ,24 ]
Velasco-Torrijos, Trinidad [25 ]
Vidal, Sebastien [26 ,27 ]
Vincent, Stephane
Wennekes, Tom [28 ]
Zuilhof, Han [28 ,29 ]
Imberty, Anne [30 ]
机构
[1] Univ Milan, Dipartimento Chim Organ & Ind, I-20133 Milan, Italy
[2] Univ Milan, Ctr Eccellenza CISI, I-20133 Milan, Italy
[3] CSIC, Ctr Invest Biol, Madrid 28040, Spain
[4] Univ Parma, Dipartimento Chim, I-43100 Parma, Italy
[5] Univ Naples Federico II, Dept Chem Sci, I-80126 Naples, Italy
[6] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
[7] Inst Biol Struct, F-38027 Grenoble 1, France
[8] Univ Helsinki, Dept Biosci, FI-00014 Helsinki, Finland
[9] Univ Dusseldorf, Forschungszentrum Julich, Inst Mol Enzyme Technol, D-42425 Julich, Germany
[10] Bangor Univ, Sch Chem, Bangor LL57 2UW, Gwynedd, Wales
[11] Univ Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, Germany
[12] CIC BiomaGUNE, Lab GlycoNanotechnol, San Sebastian 20009, Spain
[13] CIBER BBN, San Sebastian 20009, Spain
[14] Univ Nat Resources & Life Sci, NanoGlycobiol Unit, Dept NanoBiotechnol, A-1190 Vienna, Austria
[15] Natl Univ Ireland, Sch Chem, Galway, Ireland
[16] Univ Florence, Dipartimento Chim, I-50019 Sesto Fiorentino, Italy
[17] Univ Coll Dublin, UCD Sch Chem & Chem Biol, Ctr Synth & Chem Biol, Dublin 4, Ireland
[18] Univ Milano Bicocca, I-20126 Milan, Italy
[19] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Dept Med Chem & Chem Biol, NL-3508 TB Utrecht, Netherlands
[20] Univ Grenoble 1, UMR CNRS 5250, Dept Chim Mol, F-38041 Grenoble, France
[21] Univ Grenoble 1, ICMG FR 2607, F-38041 Grenoble, France
[22] Univ Seville, CSIC, Inst Invest Quim, Glycosyst Lab, Seville 41092, Spain
[23] Univ Leeds, Sch Chem, Leeds LS2 9JT, W Yorkshire, England
[24] Univ Leeds, Astbury Ctr Struct Mol Biol, Leeds LS2 9JT, W Yorkshire, England
[25] Natl Univ Ireland, Dept Chem, Maynooth, Kildare, Ireland
[26] Univ Lyon 1, CNRS, Inst Chim & Biochim Mol & Supramol UMR 5246, F-69622 Villeurbanne, France
[27] Univ Namur FUNDP, Dept Chim, Chim Bioorgan Lab, B-5000 Namur, Belgium
[28] Wageningen Univ, Organ Chem Lab, NL-6703 HB Wageningen, Netherlands
[29] King Abdulaziz Univ, Dept Chem & Mat Engn, Jeddah 21413, Saudi Arabia
[30] Univ Grenoble, Ctr Rech Macromol Vegetales CERMAV CNRS, F-38041 Grenoble, France
基金
英国工程与自然科学研究理事会;
关键词
FIMBRIATED ESCHERICHIA-COLI; PROTEIN-CARBOHYDRATE INTERACTIONS; PSEUDOMONAS-AERUGINOSA; HIGH-AFFINITY; DC-SIGN; BACTERIAL LECTIN; STRUCTURAL BASIS; GLYCOPEPTIDE DENDRIMERS; STREPTOCOCCUS-SUIS; CHOLERA-TOXIN;
D O I
10.1039/c2cs35408j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multivalency plays a major role in biological processes and particularly in the relationship between pathogenic microorganisms and their host that involves protein-glycan recognition. These interactions occur during the first steps of infection, for specific recognition between host and bacteria, but also at different stages of the immune response. The search for high-affinity ligands for studying such interactions involves the combination of carbohydrate head groups with different scaffolds and linkers generating multivalent glycocompounds with controlled spatial and topology parameters. By interfering with pathogen adhesion, such glycocompounds including glycopolymers, glycoclusters, glycodendrimers and glyconanoparticles have the potential to improve or replace antibiotic treatments that are now subverted by resistance. Multivalent glycoconjugates have also been used for stimulating the innate and adaptive immune systems, for example with carbohydrate-based vaccines. Bacteria present on their surfaces natural multivalent glycoconjugates such as lipopolysaccharides and S-layers that can also be exploited or targeted in anti-infectious strategies.
引用
收藏
页码:4709 / 4727
页数:19
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