Spelling suggestions: "subject:"bectin A"" "subject:"alectin A""
1 |
Distribution of N-acetyl-α-D-galactosamine (GalNAc) in normal and malignant oral epitheliumGriffin, Raymond Leonard January 2002 (has links)
In this project, the N-acetyl-ex-D-galactosamine (GalNAc) binding lectin from the green marine alga Codium fragile ssp. tomentosoides (C. fragile) was purified and techniques developed to label the lectin for visualisation by light and electron microscopy and electrophoresis. This represents the first time a histochemical reagent has been developed from a marine alga. The new reagent was initially assessed for transmission electron microscopy using human blood group A1 erythrocytes. A novel method gave a topographical view, and showed the distribution of gold particles on the surface of erythrocytes. The pattern of C. fragile lectin binding to pig normal oral epithelium was studied in the environmental scanning electron microscope to avoid charging artefact, using paraffin wax sections of pig normal epithelium stained with C. fragile lectin-gold conjugate enhanced with silver. X-ray micro analysis demonstrated lectin binding on the plasma membrane surface of epithelial cells at cells to cell contacts suggesting binding to cellular adhesion molecules. Biotinylated lectins binding GalNAc were used to investigate, identify and compare the binding of lectins in pig normal oral epithelium and altered glycoconjugates in cultured malignant cells from human oral tumours, using lectin histochemistry in the light microscope. Lectin from C. fragile was compared with Dolichos biflorus, a lectin from plants, and Helix pomatia (HP A) from snails. Although each lectin binds GalNAc it was shown that their binding pattern to pig normal oral epithelium was different, demonstrating that these lectins could be used to identify altered cellular glycosylation in the normal cellular maturation process. Cultured human oral tumour cells from different grades of malignancy were investigated using this panel of lectins. Binding of GalNAc specific lectins to cultured tumour cells changed in relation to their level of differentiation. This discriminating capability of GalNAc specific lectins offers exciting potential as indicators of tumour prognosis in human oral epithelial tumours. The lectins from C. fragile and HP A gave very similar staining results using histochemistry. Binding of these lectins to cell membrane glycoproteins was investigated using electrophoresis to show that C. fragile lectin binds to more and different cell membrane glycoproteins than lectin from HP A, but did not bind to purified CD44, excluding this adhesion molecule as a candidate for binding these lectins.
|
2 |
The structure and function of human soluble CD23Grundy, Gabrielle Jane January 2001 (has links)
No description available.
|
3 |
Structural Studies On Three-Fold Symmetric Plant LectinsSharma, Alok 05 1900 (has links) (PDF)
Lectins, multivalent carbohydrate-binding proteins of non-immune origin, have the unique ability to decode the information contained in complex carbohydrate structures of glycoproteins and glycolipids by stereo-specifically recognizing and binding to carbohydrates and carbohydrate linkages. The ubiquitous distribution of lectins in all forms of life and viruses along with their involvement in various biological processes such as cell-cell communication, host-pathogen interaction, cancer metastasis, embryogenesis, tissue development and mitogenic stimulation further emphasizes the importance of lectins in biological systems. Although not much is known about the endogenous roles of plant lectins, they constitute the most thoroughly studied class of lectins. On the basis of their subunit folds plant lectins have been divided in six major classes. They include jelly roll fold lectins (or legume lectins), hevein domain lectins (or cereal lectins), β-trefoil fold lectins, β-prism II fold lectins (or bulb lectins), β-prism I fold lectins and the most recently discovered lectin homologous to cyanovirin-N (http://www.cermav.cnrs.fr/lectines). Interestingly, of these, lectin subunits harbor an approximate three-fold symmetry in three cases and each subunit is believed to have evolved through successive gene duplication, fusion and divergent evolution. One of the major research activities in this laboratory involves structural studies on plant lectins. Decades of extensive studies in the laboratory have shed light on various structural and functional aspects of lectins such as variability in quaternary association, lectin-carbohydrate interactions, strategies for generating ligand specificity and multivalency. Furthermore, the β-prism I fold was first identified as a lectin fold in this laboratory through the X-ray analysis of the methyl-α-galactose complex of jacalin, one of the two lectins from the seeds of Artocarpus integrifolia. Subsequently, many other lectins with the same fold have been structurally characterized here and else where (http://www.cermav.cnrs.fr/lectines). They include mannose specific tetrameric artocarpin and dimeric banana lectin studied in this laboratory. Also investigated here is the structure of first dimeric β-prism II fold lectin, namely, garlic lectin. The subsequent work, carried out by the author, on the structure and dynamics of three-fold symmetric lectins form the subject matter of this thesis.
Different web-servers available at NCBI and EXPASY web sites were used for sequence annotation studies. MRBAYES and MEGA were used for phylogenetic analysis. Molecular dynamics (MD) simulations were carried out using the simulation package GROMACS v.3.3.1. OPLS-AA/L and GLYCAM-06 force fields were used for proteins and carbohydrates respectively. Simulations were performed in explicit water system with TIP4P water model under NPT conditions with unit dielectric constant. The hanging drop method was used for crystallizing banana lectin and its complexes. Intensity data were collected on a MAR 345 image plate mounted on a Rigaku RU200 rotating-anode X-ray generator. The Oxford cryosystem was used when collecting data at low temperature. The data were processed using DENZO and SCALEPACK of HKL suite of programs. The structure factors from the processed data were calculated using TRUNCATE of CCP4 suite of programs. The molecular replacement program MOLREP was used for structure solution. Structure refinements were carried out using the CNS software package and REFMAC of CCP4. Model building was done using the molecular graphics program COOT. INSIGHT II, ALIGN, CONTACT, MUSTANG and SC of CCP4 were used for analysis of structural features. PROCHECK and web-server MOLPROBITY were used for the validation of the refined structures.
The β-prism II fold lectins of known structure, all from monocots, invariably have three carbohydrate-binding sites in each subunit / domain. Until recently, β-prism I fold lectins of known structure were all from dicots and they exhibited one carbohydrate-binding site per subunit / domain. However, the recently determined structure of the β-prism I fold lectin from banana, a monocot, has two very similar carbohydrate-binding sites. This prompted a detailed analysis of all the sequences appropriate for the two lectin folds and which carry one or more relevant carbohydrate-binding motifs. The recent observation of a β-prism I fold lectin, griffithsin, with three binding sites in each domain further confirmed the need for such an analysis. The detailed sequence and phylogenetic analysis of all the β-prism I fold lectin or lectin-like sequences, available then, with particular attention to their carbohydrate-binding sites in them, in conjunction with the analysis of available three-dimensional structures demonstrate substantial diversity in the number of binding sites, unrelated to the taxonomical position of the plant source. However, the number of binding sites and the symmetry within the sequence exhibit reasonable correlation. The distribution of the two families of β-prism fold lectins among plants and the number of binding sites in them, appear to suggest that both of them arose through successive gene duplication, fusion and divergent evolution of the same primitive carbohydrate-binding motif involving a Greek key. Analysis with sequences in individual Greek keys as independent units lends further support to this conclusion. It would seem that the prepondence of three carbohydrate-binding sites per domain in monocot lectins, particularly those with the β-prism II fold, is related to the role of plant lectins in defence.
Jacalin is the most thoroughly studied β-prism I fold lectin. A wealth of structural and thermodynamic data, mostly from this laboratory, led to a thorough characterization of carbohydrate-recognition in the case of jacalin. One aspect of jacalin that has not been investigated so far was its dynamics. The issue was addressed through reasonably long MD simulations, in explicit solvent system using all atom force field, of all the jacalin-carbohydrate complexes of known structure, models of unliganded molecules derived from the complexes and also models of relevant complexes where X-ray structures are not available. Results of the simulations and the available crystal structures involving jacalin permit delineation of the relatively rigid and flexible regions of the molecule and the dynamical variability of the hydrogen bonds involved in stabilizing the structure. Local flexibility appears to be related to solvent accessibility. Hydrogen bonds involving side chains and water bridges involving buried water molecules appear to be important in the stabilization of loop structures. The lectin-carbohydrate interactions observed in crystal structures, the average parameters pertaining to them derived from simulations, energetic contribution of the stacking residue estimated from quantum mechanical calculations and the scatter of the locations of carbohydrate and carbohydrate-binding residues, are consistent with the known thermodynamic parameters of jacalin-carbohydrate interactions. The simulations, along with X-ray results, provide a fuller picture of carbohydrate binding by jacalin than provided by crystallographic analysis alone. The simulations confirm that in the unliganded structures water molecules tend to occupy the positions occupied by carbohydrate oxygens in the lectin-carbohydrate complexes. Population distributions in simulations of the free lectin, the ligands and the complexes indicate a combination of conformational selection and induced fit.
Mannose-specific β-prism I fold lectins, like lectins belonging to other plant families, exhibit interesting variability in their quaternary association. Mannose specific artocarpin and MornigaM are tetrameric, heltuba is octameric in the crystal structure and banana lectin and calsepa are dimeric. The modes of the dimerization in the last two are however, entirely different. This variability was explored through modelling and molecular dynamics simulations based on the known three-dimensional structures. This study, which combines computational approaches and results of X-ray analyses, provides valuable insights into the origin of the variability in quaternary association. MD simulations on individual subunits and the oligomers provide insights into the changes in the structure brought about in the protomers on oligomerization, including swapping of the N-terminal stretch in one instance. The regions which undergo changes also tend to exhibit dynamic flexibility during MD simulations. The internal symmetries of individual oligomers are substantially retained during the calculations. Simulations were also carried out on models using all possible oligomers employing the four different protomers. The unique dimerization pattern observed in calsepa could be traced to unique substitutions in a peptide stretch involved in dimerization. The impossibility of a specific mode of oligomerization involving a particular protomer is often expressed in terms of unacceptable steric contacts or dissociation of the oligomer during simulations. The calculations also lead to a rationale for the observation of a heltuba tetramer in solution although the lectin exists as an octamer in the crystal, in addition to providing insights into relations among evolution, oligomerization and ligand binding.
The known crystal structures of banana lectin in its native and ligand bound forms revealed interesting features including the presence of two functional carbohydrate-binding sites per subunit. However, some confusion remained on the role of glycosidic linkage in carbohydrate-binding. The three crystal structures reported in this thesis provide information on details of the interactions of mannose and mannosylα-1,3-mannose with banana lectin and evidence for the binding of glucosyl-α-1,2glucose to the lectin. The known structures involving the lectin include a complex with glucosyl-β-1,3-glucose. Modelling studies on the three disaccharide complexes with the reducing end and the non-reducing end at the primary binding site are also presented here. The results of the X-ray and modelling studies show that the disaccharides with an α-1,3 linkage prefers to have the non-reducing end at the primary binding site while the reducing end is preferred at the site when the linkage is β-1,3 in mannose/glucose specific β-prism I fold lectins. In the corresponding galactose-specific lectins, however, α-1,3 linked disaccharides cannot bind the lectin with the non-reducing end at the primary binding site on account of steric clashes with an aromatic residue which occurs only when the lectin is galactose-specific. MD simulations based on the known structures involving banana lectin enrich the information on lectin-carbohydrate interactions obtained from crystal structures. They demonstrate that conformational selection as well as induced fit operate when carbohydrates bind to banana lectin.
Snake gourd seed lectin (SGSL) isolated from Trichosanthes anguina is a glycosylated, galactose-specific, non-toxic lectin similar to type II ribosome inactivating proteins (RIPs) with a molecular weight of ~53kDa. It was established through preliminary X-ray studies that chain A with molecular weight of ~23kDa adopts the same fold as that of type I RIPs and the toxic chain of type II RIPs. Chain B with molecular weight ~32kDa has two β-trefoil fold domains and is responsible for the lectin activity of the protein. The two chains are connected with a disulphide bond. The sequence of the protein could not be determined using conventional methods despite extensive effort. It was derived from X-ray data at 2.4 Å resolution, which was used for structure analysis. The non-toxicity of SGSL appears to result from a combination of changes in the catalytic site in chain A and sugar-binding site in chain B. Detailed analysis of the sequences of type II RIPs of known structure and their homologues with unknown structure, provide valuable insights into the evolution of this class of proteins. It also indicates some variability in carbohydrate-binding sites, which appears to contribute to different levels of toxicity exhibited by lectins from various sources.
In addition to the work on plant lectins, the author was also involved in studies on the crystal structures of the adipic acid complexes of L- and DL-Lysine. This investigation is presented in an appendix.
A part of the work presented in the thesis has been reported in the following
publications.
Sharma, A., Thamotharan, S., Roy, S., & Vijayan, M. (2006). X-ray studies of
crystalline complexes involving amino acids and peptides. XLIII. Adipic acid
complexes of L- and DL-lysine. Acta Cryst, C62, o148-o152.
Sharma, A., Chandran, D., Singh, D.D., & Vijayan, M. (2007). Multiplicity of
carbohydrate-binding sites in beta-prism fold lectins: occurrence and possible
evolutionary implications. J Biosci, 32, 1089-1110.
Sharma, A., Sekar, K., & Vijayan, M. (2009). Structure, dynamics, and interactions of
jacalin. Insights from molecular dynamics simulations examined in conjunction
with results of X-ray studies. Proteins, 77, 760-777.
|
4 |
Variability and modification of the lectins of some members of the papilionoideaeSpencer, I. W. January 1984 (has links)
No description available.
|
5 |
Studies on the modular organization of human properdin and C1q of the complement pathwayPerdikoulis, Michael V. January 1999 (has links)
No description available.
|
6 |
Activation of the human complement system via the MBL-MASPs complexBradley, Mayumi January 2002 (has links)
No description available.
|
7 |
Glycomics : integration of lectin and gene expression microarray dataPilobello, Kanoelani Takaishi 13 October 2011 (has links)
Glycomics is the systematic study of glycosylation in the context of a whole cell or organism. Glycosylated proteins are estimated to make up 50% of all proteins and cover the outside of the cell. Functional roles in glycosylation have been noted in pathogenesis, metastasis, and embryogenesis. However, the structure of these carbohydrates has been difficult to study due to the chemical nature of carbohydrates. Lectins, carbohydrate binding proteins excluding antibodies and enzymes, can be utilized to study glycosylation in a high throughput manner using a microarray format. Glycans, the carbohydrates attached to a protein or lipid, are not synthesized from a template. They are added co- or post-translationally by a concerted set of enzymes in the secretory pathway. In addition, the glycan structures may be altered by metabolism or trafficking.
Cell type specific glycosylation has long been hypothesized due to observations of bacteria homing to tissues. We use lectin microarray technology to define the glycosylation in a subset of the NCI-60, a set of cell lines from different tissues. Using a customized gene expression microarray, we identify cell type dependent glycosylation genes and observe evidence of cell type dependent spliceforms for an O-glycosylated mucin. Data from the lectin microarray and a published gene expression data set were integrated using Generalized Singular Value Decomposition (GSVD), a linear matrix decomposition method. We have successfully decomposed the data into 3 cell type dependent meta patterns that segregate by glycosylation family. Correlation projection of the genes and subsequent gene ontology enrichment suggests that genes in different pathways covary with the types of glycosylation. An inverse relationship was revealed for the N- glycosylation pattern between the SVD of the lectins and the GSVD of the genes and lectins together. Whereas, the relationship was correlative for O-glycosylation, which was clearly illustrated in biplots. This work argues that types of glycosylation are regulated by different mechanisms in different cell types. / text
|
8 |
Glycobiology of Ticks and Tick-Borne Pathogens. Glycans, Glycoproteins, and Glycan-Binding Proteins. / Glycobiology of Ticks and Tick-Borne Pathogens. Glycans, Glycoproteins, and Glycan-Binding Proteins.ŠTĚRBA, Ján January 2012 (has links)
The proposed thesis brings new information on several aspects of tick glycobiology - tick N-glycans, tick lectins, and glycosylation of the tick-borne pathogen, Lyme disease spirochetes Borrelia burgdorferi s.l.
|
9 |
Advances in protein microarray technology for glycomic analysisPropheter, Daniel Champlin 13 October 2011 (has links)
The cell surface is enveloped with a myriad of carbohydrates that form complex matrices of oligosaccharides. Carbohydrate recognition plays crucial and varying roles in cellular trafficking, differentiation, and bacterial pathogenesis. Lectin microarray technology presents a unique platform for the high-throughput analysis of these structurally diverse classes of biopolymers. One significant hinderance of this technology has been the limitation imposed by the set of commercially available plant lectins used in the array. To enhance the reproducibility and scope of the lectin panel, our lab generated a small set of bacteria-derived recombinant lectins.
This dissertation describes the unique advantages that recombinant lectins have over traditional plant-derived lectins. The recombinant lectins are expressed with a common fusion tag, glutathione-S-transferase (GST), which can be used as an immobilization handle on glutathione (GSH)-modified substrates. Although protein immobilization via fusion tags in a microarray format is not novel, our work demonstrates that protein activity through site-specific immobilization is enhanced when the protein is properly oriented. Although orientation enhanced the activity of our GST-tagged recombinant lectins, the GSH-surface modification precluded the printing of non-GST-tagged lectins, such as the traditional plant lectins, thus limiting the structural resolution of our arrays. To solve this issue, we developed a novel print technique which allows the one-step deposition and orientation of GST-tagged proteins in a microarray format. To expand our view of the glycome, we further adapt this method for the in situ orientation of unmodified IgG and IgM antibodies using GST-tagged antibody-binding proteins.
Another advantage of recombinant lectins is in the ease of genomic manipulation, wherein we could tailor the binding domain to bind a different antigen. We demonstrate this by producing non-binding variants of the recombinant lectins to act as negative controls in our microarrays. Along with the non-binding variants, we developed a lectin displayed on the surface of phage. In the hopes generating more novel lectins, I will describe our current efforts of lectin evolution using phage-displayed GafD. By generating novel tools in lectin microarray technology, we enhance our understanding of the role of carbohydrates on a global scale. / text
|
10 |
Cristalização e resolução de estrutura das proteínas Canavalia gladiata lectin (CGL) e Canavalia marítima lectin (CML) complexadas ao açúcar manose 1-6 manoseVacari, Fernando Celestino Moreira [UNESP] 29 January 2010 (has links) (PDF)
Made available in DSpace on 2014-06-11T19:22:55Z (GMT). No. of bitstreams: 0
Previous issue date: 2010-01-29Bitstream added on 2014-06-13T19:49:18Z : No. of bitstreams: 1
vacari_fcm_me_sjrp.pdf: 2872179 bytes, checksum: 1bf0cdb8298278a7abef6a8501917773 (MD5) / Este trabalho teve por objetivo cristalizar e resolver tridimensionalmente as estruturas das proteínas Canavalia gladiata lectin (CGL) e Canavalia marítima lectin (CML), ambas complexadas com o açúcar manose 1-6 manose, encontradas em sementes de leguminosas. Para o processo de cristalização foi utilizado um kit de cristalização, contendo 96 soluções previstas pelo método de cristalização da matriz esparsa, denominado Screen Index (Hampton Research). Para o processo de resolução de estrutura foi utilizado diversos métodos computacionais dentre eles, o programa CCP4 (Collaborative Computational Project n° 4). Já com a estrutura resolvida, pode-se observar o sítio de ligação da proteína e identificar quais aminoácidos fazem parte do mesmo; calcular o RMSD médio entre as estruturas nativa e complexada com o açúcar manose 1-6 manose; comparar os sítios de ligação das proteínas CGL e CML complexadas com os açúcares man 1-2 man, man 1-3 man, man 1-4 man e man 1-6 man. Enfim, o trabalho colaborou para que duas novas estruturas fossem depositadas no banco de dados PDB (Protein Data Bank), para que futuros pesquisadores possam realizar estudos utilizando essas estruturas já resolvidas. / This study aimed to crystallize and solve the three-dimensional structures of proteins Canavalia gladiata lectin (CGL) e Canavalia maritime lectin (CML), both complexed with sugar manose 1-6 manose, found in legume seed. For the crystallization process was used a kit of crystallization, containing 96 solutions provided by the method of crystallization of the sparse matrix, called Screen Index (Hampton Research). For the process of resolution structure was used several computation methods among them, the program CCP4 (Collaborative Computational Project n° 4). Now with the structure resolved, can observe the binding siti of protein and amino acids to identify which part of the same; calculate the avarage RMSD betweem the native and complexed structures with the sugar manose 1-6 manose; compare the binding sites of CGL and CML proteins complexed with sugars man 1-2 man, man 1-3 man, man 1-4 man and man 1-6 man. Finally, the work helped the two new structures were deposited in the PDB database, for future researchers to conduct studies using these structures already solved.
|
Page generated in 0.0518 seconds