By V.M. Rosenoer
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133. Van Oss, C. J. (1970) Ultrafiltration membranes. In: Progress in Separation and Purification, E. S. Perry, editor, pp. 97-132. Wiley, New York. 134. Pedersen, K. O. (1962) Exclusion chromatography. Arch. Biochem. , suppl. 1, 157-168. 135. Pedersen, K. O. and L. O. Andersson (1963) Fractionation of serum albumin on sephadex. Acta Chem. Scand. 17, 871. 136. Determann, H. (1969) Gel Chromatography, 2nd edition. Springer-Verlag, New York. 137. Altgelt, K. H. and L. Segal (1971) Gel Permeation Chromatography.
261-270. Elsevier, New York. 148. McMenamy, R. , H. M. Dintzis and F. Watson (1971) Cyanogen bromide fragments of human serum albumin. / . Biol. Chem. 246, 4744-4750. 149. McMenamy, R. H. and Y. Lee (1967) Microheterogeneity in albumin: a contaminant. Arch. Biochem. Biophys. Ill, 635-643. % The method employed precipitation with PEG and sequential chromatography on DEAE Sepharose, SP Sephadex and desalting on Sephadex G-25. 150. Curling, J. , J. Berglof, L. O. Lindquist and S. Eriksson (1977) Large scale Chromatographie procedure for the purification of human plasma albumin.
E. 102-133, 288-313 and 486-511) indicates that these segments are probably non-helical. e. segments 62-81, 251-270 and 445-464). None of these segments contains a Pro residue in either BSA or HSA. The simplest hypothesis is that this helix would lie antiparallel and in contact with the adjacent helix of the large loop above, thus fusing the small double loop subdomain with the subdomain above it. Because of the 100° rotation between the adjacent Cys residues, the three helices would form a troughlike structure.