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. 2018 Oct 25;27(11):1923–1941. doi: 10.1002/pro.3501

Table 2.

Secondary structure characterization by circular dichroism spectroscopy

A. nMOMP serovars extracted from adherent HeLa cells
Serovar Serovar D,E,F, and J
Muridarum (%) D (%) E (%) F (%) J (%) Mean (%) SD (%)
Helix 11.6 19.0 22.0 20.3 19.0 20.1 1.4
Antiparallel 31.1 12.1 11.5 11.5 12.1 11.8 0.3
Parallel 5.8 12.1 11.2 11.8 12.1 11.8 0.4
Beta‐turn 17.3 17.6 17.7 17.3 17.6 17.6 0.1
Rndm. coil 34.1 39.2 37.5 39.0 39.2 38.7 0.8
All β‐sheet 36.9 24.2 22.8 23.3 24.2 23.6 0.7
B. Chlamydia trachomatis Serovar E nMOMP extracted from various suspension cells
Suspension cell line
CAP (%) CLDK (%) CHO (%) HeLa (%) Mean (%) SD (%)
Helix 29.6 27.3 23.7 28.1 27.2 2.5
Antiparallel 11.7 12.1 13.8 11.7 12.3 1.0
Parallel 9.1 9.6 10.2 9.4 9.6 0.4
Beta‐turn 17.5 17.3 17.3 17.2 17.3 0.1
Rndm. coil 32.1 33.8 35.0 33.6 33.6 1.2
All β‐sheet 20.8 21.7 24.0 21.1 21.9 1.5

Secondary structure composition of nMOMP calculated by deconvolution of circular dichroism spectra. (A) Chlamydia muridarum and C. trachomatis Serovars D, E, F, and J nMOMP obtained from adherent HeLa cells. (B) Chlamydia trachomatis Serovar E nMOMP obtained from infected suspension cell lines.