The crystal structure of poly(L-hydroxyproline) (PHypro) with trans pl
anar conformation of the peptide group is reexamined. The electron dif
fraction pattern obtained from solution-grown triangular single crysta
ls confirms the unit-cell geometry determined by Sasisekharan (Act a C
rystallogr. 1959, 12, 903) (trigonal unit cell with parameters a = b =
12.3 Angstrom and c = 9.15 Angstrom, three left-handed 3-fold helices
per unit cell). Analysis of the diffraction data and the single-cryst
al morphology indicates that PHypro crystallizes in a frustrated struc
ture characterized by the fact that the azimuthal orientation of one o
f the helices differs significantly from that of the other two. Such a
n arrangement is, however, compatible with hydrogen bonding between th
e hydroxyl groups and the carbonyl groups of the neighbor helices. It
further accounts for the highly unusual triangular morphology of solut
ion-grown single crystals.