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. Author manuscript; available in PMC: 2010 Jul 31.
Published in final edited form as: J Mol Biol. 2009 Jun 3;390(5):863–878. doi: 10.1016/j.jmb.2009.05.076

Figure 3.

Figure 3

(A) Size exclusion chromatography profiles of mR1(core) purified with (—) and without (---) addition of 50 µM Zn2+. The chromatographic profiles are from a preparative 120 ml Superdex 200 column and monitored by UV absorption. The buffer for mR1(core) purified with added Zn2+ contained 50 µM Zn2+ and 0.5 M NaCl, while the buffer for mR1(core) purified in the absence of added Zn2+ contained 0.5 M NaCl and was treated with Chelex to remove any adventitious metals. (B) SDS-PAGE of mR1(core) purified in the absence of added Zn2+. Fractions collected from SEC are A (elution volume 68.2–71.2 mL); B (elution volume 59.2–61.2 mL); and C (elution volume 45.2–48.2 mL). These fractions correspond to lanes A, B, and C on the gel. (C) SDS-PAGE of mR1(core) purified in the presence of Zn2+ shows the characteristic dimer band in Fraction B. Fraction B purified in the presence of added Zn2+ corresponds to the SEC elution volume collected for Fraction B prepared in the absence of added Zn2+.