8C3E

Engineered mini-protein LCB2 (blocking ligand of SARS-Cov-2 spike protein)

8C3E の概要

• エントリーDOI: 10.2210/pdb8c3e/pdb
• 分子名称: Engineered protein LCB2, GLYCEROL (3 entities in total)
• 機能のキーワード: sars-cov-2, mini-protein, antiviral, blocking ligand, antiviral protein
• 由来する生物種: synthetic construct
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 7297.23

構造登録者

Korban, S.A.,Mikhailovskii, O.V.,Luzik, D.A.,Gurzhiy, V.V.,Levkina, A.D.,Kharkov, B.B.,Skrynnikov, N.R. (登録日: 2022-12-23, 公開日: 2023-04-12, 最終更新日: 2025-07-23)

主引用文献

Korban, S.A.,Mikhailovskii, O.,Gurzhiy, V.V.,Podkorytov, I.S.,Skrynnikov, N.R.
Using multiple computer-predicted structures as molecular replacement models: application to the antiviral mini-protein LCB2.
Iucrj, 12:488-501, 2025

PubMed Abstract: In this report, we describe a set of structures of the engineered protein LCB2 that has been solved starting from different computer-predicted molecular replacement (MR) models. We found that AlphaFold3, AlphaFold2, MultiFOLD, Rosetta, RoseTTAFold and trRosetta all produced successful MR models for this three-helix bundle 58-residue protein, while some of the older predictors failed. To assign B factors in the MR models we used the predictor-generated confidence scores or, as a convenient alternative, the accessible surface area (ASA) values. The process of multi-start structure determination using Coot and Phenix demonstrated good convergence, leading to six structures within 0.25 Å (all-atom RMSD) of each other. Of note, structural differences between the computer-predicted MR models and the final structures can be largely attributed to a single specific crystal contact. Comparing the six structural solutions, we observe that a number of surface side chains have been solved with different conformations. Interestingly, for each individual structure the electron density is consistent with a single rotameric state and offers no direct evidence of conformational heterogeneity. Strictly speaking, this behavior constitutes a case of model bias; we argue, however, that it represents a benign side of model bias. Specifically, when we use a model where the side-chain conformation corresponds to one of the actual (significantly populated) rotameric states, this leads to an enhancement of the electron density for this particular conformation. Conversely, when we use a model with an irrelevant (low-population) side-chain conformation, it fails to produce the matching electron density. We thus conclude that the six LCB2 structures obtained in this study can be grouped into a multiconformer ensemble, where structural variations are representative of protein's conformational dynamics. Indeed, using this six-member ensemble leads to a significant drop in R and R compared with the individual solutions. This interpretation was also supported by our MD simulations of the LCB2 crystal.

PubMed: 40549150
DOI: 10.1107/S2052252525005123

実験手法

X-RAY DIFFRACTION (2.1 Å)