7MG3

Concanavalin A crystallized in the presence of H2N-ATAT

7MG3 の概要

• エントリーDOI: 10.2210/pdb7mg3/pdb
• 関連するPDBエントリー: 7MG1
• 分子名称: Concanavalin-A, MANGANESE (II) ION, CALCIUM ION, ... (4 entities in total)
• 機能のキーワード: lectin, sugar binding protein-dna complex, sugar binding protein/dna
• 由来する生物種: Canavalia ensiformis (Jack bean, Dolichos ensiformis); 詳細
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 25717.40

構造登録者

Partridge, B.E.,Winegar, P.H.,Mirkin, C.A. (登録日: 2021-04-12, 公開日: 2021-06-16, 最終更新日: 2023-10-18)

主引用文献

Partridge, B.E.,Winegar, P.H.,Han, Z.,Mirkin, C.A.
Redefining Protein Interfaces within Protein Single Crystals with DNA.
J.Am.Chem.Soc., 143:8925-8934, 2021

PubMed Abstract: Proteins are exquisite nanoscale building blocks: molecularly pure, chemically addressable, and inherently selective for their evolved function. The organization of proteins into single crystals with high positional, orientational, and translational order results in materials where the location of every atom can be known. However, controlling the organization of proteins is challenging due to the myriad interactions that define protein interfaces within native single crystals. Recently, we discovered that introducing a single DNA-DNA interaction between protein surfaces leads to changes in the packing of proteins within single crystals and the protein-protein interactions (PPIs) that arise. However, modifying specific PPIs to effect deliberate changes to protein packing is an unmet challenge. In this work, we hypothesized that disrupting and replacing a highly conserved PPI with a DNA-DNA interaction would enable protein packing to be modulated by exploiting the programmability of the introduced oligonucleotides. Using concanavalin A (ConA) as a model protein, we circumvent potentially deleterious mutagenesis and exploit the selective binding of ConA toward mannose to noncovalently attach DNA to the protein surface. We show that DNA association eliminates the major PPI responsible for crystallization of native ConA, thereby allowing subtle changes to DNA design (length, complementarity, and attachment position) to program distinct changes to ConA packing, including the realization of three novel crystal structures and the deliberate expansion of ConA packing along a single crystallographic axis. These findings significantly enhance our understanding of how DNA can supersede native PPIs to program protein packing within ordered materials.

PubMed: 34096291
DOI: 10.1021/jacs.1c04191

実験手法

X-RAY DIFFRACTION (1.6 Å)