Hayashi F, Endo S, Arata Y, Shimizu A, Kyogoku Y
Institute for Protein Research, Osaka University, Japan.
Biochemistry. 1989 May 2;28(9):3976-81. doi: 10.1021/bi00435a052.
The results of photo-CIDNP measurements of Bence Jones proteins, immunoglobulins, and their proteolytic fragments are reported. The CIDNP spectra of constant region CL fragments, which were derived from lambda-type Bence Jones proteins with three different isotypes, gave polarizations originating from two Tyr and one Trp residues. From comparisons of the results obtained by using lambda-type Bence Jones proteins that possess the known amino acid sequences with those for the CL fragments, it was concluded that the CIDNP signals observed in the case of Bence Jones proteins are all due to the hypervariable region. On the basis of the results obtained by using IgG1, IgG2, IgG3, and IgG4 myeloma proteins along with their Fab, Fc, and pFc' fragments, it was concluded that CIDNP signals for the Fab region all originate from the variable region. The Fc region gives two Tyr polarizations, one of which has been assigned to Tyr-296. We have also shown that the second Tyr signal is due to Tyr-373. Interaction of Fc and staphylococcal protein A has also been examined by the CIDNP technique.
报道了对本-周蛋白、免疫球蛋白及其蛋白水解片段进行光化学诱导动态核极化(photo-CIDNP)测量的结果。来自三种不同同种型的λ型本-周蛋白的恒定区CL片段的CIDNP光谱给出了源自两个酪氨酸(Tyr)和一个色氨酸(Trp)残基的极化。通过比较具有已知氨基酸序列的λ型本-周蛋白与CL片段的测量结果,得出结论:在本-周蛋白情况下观察到的CIDNP信号均归因于高变区。基于使用IgG1、IgG2、IgG3和IgG4骨髓瘤蛋白及其Fab、Fc和pFc'片段所获得的结果,得出结论:Fab区的CIDNP信号均源自可变区。Fc区给出两个酪氨酸极化,其中一个已确定为Tyr-296。我们还表明,第二个酪氨酸信号归因于Tyr-373。还通过CIDNP技术研究了Fc与葡萄球菌蛋白A的相互作用。