Krylov D M, Niemi G A, Dizhoor A M, Hurley J B
Department of Biochemistry and The Howard Hughes Medical Institute, University of Washington, Seattle, Washington 98195, USA.
J Biol Chem. 1999 Apr 16;274(16):10833-9. doi: 10.1074/jbc.274.16.10833.
Guanylyl cyclase activating protein (GCAP)-1 regulates photoreceptor membrane guanylyl cyclase, RetGC, in a Ca2+-sensitive manner. It contains four Ca2+-binding motifs, EF-hands, three of which are capable of binding Ca2+. GCAP-1 activates RetGC in low Ca2+ and inhibits it in high Ca2+. In this study we used deletion and substitution analysis to identify regions of GCAP-1 sequence that are specifically required for inhibition and activation. A COOH-terminal sequence within Met157 to Arg182 is required for activation but not for inhibition of RetGC. We localized one essential stretch to 5 residues from Arg178 to Arg182. Another sequence essential for activation is within the N-terminal residues Trp21 to Thr27. The region between EF-hands 1 and 3 of GCAP-1 also contains elements needed for activation of RetGC. Finally, we found that inhibition of RetGC requires the first 9 amino-terminal residues of GCAP-1, but none of the residues from Gln33 to the COOH-terminal Gly205 are specifically required for inhibition. The ability of GCAP-1 mutants to regulate RetGC was tested on total guanylyl cyclase activity present in rod outer segments. In addition, the key mutants were also shown to produce similar effects on recombinant bovine outer segment cyclases GC1 and GC2.
鸟苷酸环化酶激活蛋白(GCAP)-1以钙敏感的方式调节光感受器膜鸟苷酸环化酶RetGC。它含有四个钙结合基序,即EF手结构,其中三个能够结合钙离子。GCAP-1在低钙条件下激活RetGC,在高钙条件下抑制它。在本研究中,我们使用缺失和置换分析来确定GCAP-1序列中抑制和激活所特需的区域。Met157至Arg182内的一个羧基末端序列是激活RetGC所必需的,但不是抑制所必需的。我们将一个必需片段定位到从Arg178到Arg182的5个残基处。另一个激活所必需的序列在N端残基Trp21至Thr27内。GCAP-1的EF手结构1和3之间的区域也包含激活RetGC所需的元件。最后,我们发现抑制RetGC需要GCAP-1的前9个氨基末端残基,但从Gln33到羧基末端Gly205的残基都不是抑制所特需的。在视杆外段中存在的总鸟苷酸环化酶活性上测试了GCAP-1突变体调节RetGC的能力。此外,关键突变体对重组牛外段环化酶GC1和GC2也显示出类似的作用。