7T1K

Crystal structure of a superbinder Fes SH2 domain (sFes1) in complex with a high affinity phosphopeptide

7T1K の概要

• エントリーDOI: 10.2210/pdb7t1k/pdb
• 分子名称: Tyrosine-protein kinase Fes/Fps, Synthetic phosphotyrosine-containing Ezrin-derived peptide, CHLORIDE ION, ... (7 entities in total)
• 機能のキーワード: src homology 2 (sh2), superbinder, engineered, phage display, signaling protein
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 12813.27

構造登録者

Martyn, G.D.,Singer, A.U.,Veggiani, G.,Kurinov, I.,Sicheri, F.,Sidhu, S.S. (登録日: 2021-12-02, 公開日: 2022-08-24, 最終更新日: 2024-11-13)

主引用文献

Martyn, G.D.,Veggiani, G.,Kusebauch, U.,Morrone, S.R.,Yates, B.P.,Singer, A.U.,Tong, J.,Manczyk, N.,Gish, G.,Sun, Z.,Kurinov, I.,Sicheri, F.,Moran, M.F.,Moritz, R.L.,Sidhu, S.S.
Engineered SH2 Domains for Targeted Phosphoproteomics.
Acs Chem.Biol., 17:1472-1484, 2022

PubMed Abstract: A comprehensive analysis of the phosphoproteome is essential for understanding molecular mechanisms of human diseases. However, current tools used to enrich phosphotyrosine (pTyr) are limited in their applicability and scope. Here, we engineered new superbinder Src-Homology 2 (SH2) domains that enrich diverse sets of pTyr-peptides. We used phage display to select a Fes-SH2 domain variant (superFes; sFes) with high affinity for pTyr and solved its structure bound to a pTyr-peptide. We performed systematic structure-function analyses of the superbinding mechanisms of sFes and superSrc-SH2 (sSrc), another SH2 superbinder. We grafted the superbinder motifs from sFes and sSrc into 17 additional SH2 domains and confirmed increased binding affinity for specific pTyr-peptides. Using mass spectrometry (MS), we demonstrated that SH2 superbinders have distinct specificity profiles and superior capabilities to enrich pTyr-peptides. Finally, using combinations of SH2 superbinders as affinity purification (AP) tools we showed that unique subsets of pTyr-peptides can be enriched with unparalleled depth and coverage.

PubMed: 35613471
DOI: 10.1021/acschembio.2c00051

実験手法

X-RAY DIFFRACTION (1.25 Å)