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              Biopolymers                                                                                 245

              (sometimes after minor conformational changes) onto the  Within ribosomes, strong interactions between protein
              surface of another.                               and r-RNA are essential for maintenance of the structure
                Proteins, in particular, must be able to interact with  and functioning of the ribosome. Details of these interac-
              other polymers, for enzymes are involved in the synthesis  tions are not yet well understood.
              and degradation of all biopolymers. In addition, however,  Polysaccharide-polysaccharide interactions can also
              many examples are known of associations between nonen-  take place, probably involving extensive hydrogen bond-
              zymic proteins and other proteins, polysaccharides, or nu-  ing and “shape fitting” over lengths of twenty or more
              cleic acids. Muscle movement, for example, is brought  monosaccharide residues. This is important in plant cell
              aboutandcontrolledbycomplexinteractionsbetweensev-  walls where cellulose fibers are embedded in a matrix of
              eral proteins (myosin, actin, troponin, and tropomyosin)  proteins and several different polysaccharides.
              while collagen fibers are associated with both glycopro-
              teins and proteoglycans in connective tissues. Protein an-
              tibodies can bind to protein or polysaccharide antigens,  SEE ALSO THE FOLLOWING ARTICLES
              while polypeptide hormones must be recognized by their
              receptors, themselves proteins or glycoproteins. The pro-  BIOMATERIALS,SYNTHESIS,FABRICATION, AND APPLI-
              teins that interact with nucleic acids (e.g., repressors) bind  CATIONS • GLYCOPROTEINS AND CARBOHYDRATES • HY-
              to specific base sequences or secondary structures on the  DROGEN BONDS • POLYMER PROCESSING • POLYMERS,
              polymeric acids. In some cases these base sequences are  RECYCLING • POLYMERS,STRUCTURE • POLYMERS,
              almost palindromic (read the same backward or forward)  SYNTHESIS
              as in XV, and the protein molecules which bind to them
              often have two subunits so that one may bind to each strand
              of the DNA.
                                                                BIBLIOGRAPHY
                5 end ---- GT TCACTC TGAAC---- 3 end


                                                                Branden, C., and Tooze, J. (1999). “Introduction to Protein Structure,”


                3 end ---- CAAGTGAGACT T G- ---5 end             2nd ed., Garland Publishing Inc., New York.
                                                                Dey, P. M., and Harborne, J. B. (1997). “Plant Biochemistry,” Academic
                                   XV                            Press, New York.
                                                                Dumitriu, S., ed. (1998). “Polysaccharides,” Marcel Dekker, New York.
                                                                Fried, J. R. (1995). “Polymer Science and Technology,” Prentice-Hall,
                A “motif” found in several DNA-binding proteins con-  New Jersey.
                                                                Neidle, S., ed. (1998). “Oxford Handbook of Nucleic Acid Structure,”
              sists of two helices linked by a short stretch of polypeptide
                                                                 Oxford University Press, New York.
              chain in the form of a sharp bend. Such an arrangement  Voet, D., Voet, J. G., and Pratt, C. W. (1999). “Fundamentals of Bio-
              fits easily into a groove of double helical DNA.    chemistry,” John Wiley & Sons, New York.
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