Raslns: Genetically Encoded Intrabodies of Activated Ras Proteins

JOURNAL OF MOLECULAR BIOLOGY

卷:429

Article

Cetin, Mehmet¹  Evenson, William E.²  Gross, Garrett G.¹  Jalali-Yazdi, Farzad³  Krieger, Daniel²  Arnold, Don¹  Takahashi, Terry T.²  Roberts, Richard W.^1,2,3,4 

[1] Univ So Calif, Dept Mol & Computat Biol, Los Angeles, CA 90089 USA

[2] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA

[3] Univ So Calif, Mork Family Dept Chem Engn & Mat Sci, Los Angeles, CA 90089 USA

[4] USC Norris Comprehens Canc Ctr, Los Angeles, CA 90089 USA

关键词: mRNA display;    E10Fnlll;    fibronectin;    Ras;    intrabody;   

DOI  :  10.1016/j.jmb.2016.11.008

来源: Elsevier

【 摘 要 】

K- and H-Ras are the most commonly mutated genes in human tumors and are critical for conferring and maintaining the oncogenic phenotype in tumors with poor prognoses. Here, we design genetically encoded antibody-like ligands (intrabodies) that recognize active, GTP-bound K- and H-Ras. These ligands, which use the 10th domain of human fibronectin as their scaffold, are stable inside the cells and when fused with a fluorescent protein label, the constitutively active G12V mutant H-Ras. Primary selection of ligands against Ras with mRNA display resulted in an intrabody (termed Rasln1) that binds with a K-D of 2.1 mu M to H-Ras(G12V) (GTP), excellent state selectivity, and remarkable specificity for K- and H-Ras. Rasln1 recognizes residues in the Switch I region of Ras, similar to Raf-RBD, and competes with Raf-RBD for binding. An affinity maturation selection based on Rasln1 resulted in Rasln2, which binds with a K-D of 120 nM and also retains excellent state selectivity. Both of these intrabodies colocalize with H-Ras, K-Ras, and G12V mutants inside the cells, providing new potential tools to monitor and modulate Ras-mediated signaling. Finally, Rasln1 and Rasln2 both display selectivity for the G12V mutants as compared with wild-type Ras providing a potential route for mutant selective recognition of Ras. (C) 2016 Published by Elsevier Ltd.

【 授权许可】

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