Protein–carbohydrate interactions

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Carbohydrate–protein interactions form the basis of specific recognition of carbohydrates by lectins. Carbohydrates are important biopolymers and have a variety of functions. Often carbohydrates serve a function as a recognition element. That is, they are specifically recognized by other biomolecules. Proteins which bind carbohydrate structures are known as lectins. Compared to the study of protein–protein and protein–DNA interaction, it is the recent even those scientists get to know the protein–carbohydrate binding.[1]

Many of these interactions involved carbohydrates found at the cell surface, as part of a membrane glycoprotein or glycolipid. These interactions can play a role in cellular adhesion and other cellular recognition events.

Classification[edit]

Generally, there are two types of protein carbohydrate binding important in biological processes: Lectin and antibody.

Lectin[edit]

Lectin is a kind of protein that can bind to carbohydrate with their carbohydrate recognition domains (CRDs). We could use different CRD to classify them.[2]

C-type[edit]

Ca2+ is required to activate the binding. Ca2+ binds to the protein and carbohydrate by non covalent bond. Mannose-binding protein (MBP) contains the C-type CRD.

Protein carbohydrate binding.png

P-type[edit]

Two types mannose-6-phosphate can recognize phosphorylated saccharide. One is cation-dependent and the other does not require cation to activate.

I-type[edit]

I-type lectin named from the immunoglobulin-like domain. Sialoadhesin is one of the I-type lectin, which binds specifically to sialic acid.

Antibody[edit]

Most antibodies have the similar structure except the hypervariable region which is called the antigen binding site. This region is constituted by the combination of various amino acids. When the antigen is a kind of carbohydrate (Polysaccharide), the binding could be regarded as a protein-carbohydrate interaction.

Biological function[edit]

Protein–carbohydrate interactions play an important role in biological function.

  • Cell adhesion[3]
  • Signal Transduction[4]
  • Host-Pathogen Recognition[5]
  • Inflammation[6]

Methods of study[edit]

  • X-ray crystallography

Just like other organic molecule study, X-ray crystallography is a very useful tool to know the detail information on the interaction between carbohydrate and protein.[7]

  • NMR Study

By using titration, NOESY(Nuclear Overhauser Effect SpectroscopY), CIDNP experiments, the specificity and affinity of binding, association constants and equilibrium thermodynamic parameters of carbohydrate–protein binding can be studied.[8]

  • Molecular Modeling

In many cases, the conformation information is required, however, sometimes it is not able to get directly from the experiments. So the knowledge-based model building approach is used.

  • Fluorescence Spectrometry

Fluorescence spectrometry is a useful tool and has its advantages: no procedure for separation and plenty of ways to get fluorophore source: there are some of amino acids and ligands that have fluorophore after they are activated.[9]

  • Dual polarisation interferometry

Dual polarisation interferometry is a label free analytical technique for measuring interactions and associated conformational changes.[10]

Advances in the study of protein–carbohydrate binding[edit]

  • Microarray-Based Study by Metal Nanoparticle Probes

Recently, studies by using metal nanoparticle probes to detect the carbohydrate–protein interactions were reported.[11] Use of gold and silver nanoparticle probes in resonant light scattering (RLS) gives particular high sensitivity. Zhenxin Wang and coworker the same principle applied this method to detect the interaction between carbohydrate and protein.

  • Carbohydrate biosensor

As Lectin can strongly bind to specific carbohydrate, scientists develop several lectin-based carbohydrate biosensors.[12] Designed lectin contains specific groups can be detected by analytical method.

  • Isothermal Titration Calorimetry[13]

References[edit]

  1. ^ Dwek, R. A. Chem. Rev. 1996, 96, 683–720.
  2. ^ Lis, H.; Sharon, N. Chem. Rev. 1998, 98, 637–674.
  3. ^ Geijtenbeek, T.; Torensma, R.; van Vliet, S.; van Duijnhoven, G.;Adema, G.; van Kooyk, Y.; Figdor, C. Cell 2000, 100, 575–585.
  4. ^ Sacchettini, J. C.; Baum, L. G.; Brewer, C. F. Biochemistry 2001, 40,3009–3015.
  5. ^ Karlsson, K. A. Biochem. Soc. Trans. 1999, 27, 471–474.
  6. ^ Kansas, G. S. Blood 1996, 88, 3259–3287.
  7. ^ Somers, W. S.; Tang, J.; Shaw, G. D.; Camphausen, R. T. Cell 2000, 103, 467–479.
  8. ^ Povedaa, A.; Jim´enez-Barbero, J. Chem. Rev. 1998, 27, 133–143.
  9. ^ Lee, Y. C. J. Biochem. 1997, 121, 818–825.
  10. ^ Popplewell, J.F.; Swann, M.J.; Ahmed,Y.; Turnbull, J.E.; Fernig, D.G. ChemBioChem Feb 2009.
  11. ^ Gao, J.; Liu, D.; Wang, Z. Anal. Chem. 2008, 80, 8822–8827.
  12. ^ Jelinek, R.; Kolusheva, S. Chem. Rev. 2004, 104, 5987–6016.
  13. ^ Dam, T. K.; Brewer, C. F. Chem. Rev. 2002, 102, 387–430.