Rawi Reda, Kunji Khalid, Haoudi Abdelali, Bensmail Halima
Computational Sciences and Engineering Center, Qatar Computing Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University for Health Sciences, National Guards Health Affairs, Riyadh, KSA. 2, Department of Genetics and Genomics, Boston Children’s Hospital, Harvard Medical School, USA.
PLoS One. 2015 Nov 18;10(11):e0143245. doi: 10.1371/journal.pone.0143245. eCollection 2015.
The HIV-1 Env spike is the main protein complex that facilitates HIV-1 entry into CD4+ host cells. HIV-1 entry is a multistep process that is not yet completely understood. This process involves several protein-protein interactions between HIV-1 Env and a variety of host cell receptors along with many conformational changes within the spike. HIV-1 Env developed due to high mutation rates and plasticity escape strategies from immense immune pressure and entry inhibitors. We applied a coevolution and residue-residue contact detecting method to identify coevolution patterns within HIV-1 Env protein sequences representing all group M subtypes. We identified 424 coevolving residue pairs within HIV-1 Env. The majority of predicted pairs are residue-residue contacts and are proximal in 3D structure. Furthermore, many of the detected pairs have functional implications due to contributions in either CD4 or coreceptor binding, or variable loop, gp120-gp41, and interdomain interactions. This study provides a new dimension of information in HIV research. The identified residue couplings may not only be important in assisting gp120 and gp41 coordinate structure prediction, but also in designing new and effective entry inhibitors that incorporate mutation patterns of HIV-1 Env.
HIV-1包膜糖蛋白刺突是促进HIV-1进入CD4+宿主细胞的主要蛋白复合物。HIV-1的进入是一个尚未完全了解的多步骤过程。该过程涉及HIV-1包膜糖蛋白与多种宿主细胞受体之间的几种蛋白质-蛋白质相互作用,以及刺突内的许多构象变化。由于高突变率以及从巨大免疫压力和进入抑制剂中逃逸的可塑性策略,HIV-1包膜糖蛋白得以进化。我们应用了一种共进化和残基-残基接触检测方法,以识别代表所有M组亚型的HIV-1包膜糖蛋白序列中的共进化模式。我们在HIV-1包膜糖蛋白中鉴定出424对共进化残基对。大多数预测的残基对是残基-残基接触,并且在三维结构中是相邻的。此外,由于在CD4或共受体结合、可变环、gp120-gp41以及结构域间相互作用中的作用,许多检测到的残基对具有功能意义。这项研究为HIV研究提供了新的信息维度。所鉴定的残基偶联不仅可能在协助gp120和gp41的结构预测方面很重要,而且在设计纳入HIV-1包膜糖蛋白突变模式的新型有效进入抑制剂方面也很重要。