Yang Z N, Mueser T C, Kaufman J, Stahl S J, Wingfield P T, Hyde C C
Laboratory of Structural Biology Research, National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, Maryland 20892, USA.
J Struct Biol. 1999 Jun 15;126(2):131-44. doi: 10.1006/jsbi.1999.4116.
Cell membrane fusion by human (HIV) and simian (SIV) immunodeficiency viruses is mediated by the envelope glycoproteins gp120 and gp41. Although the precise mechanism of the fusion process is unknown, the ectodomain of gp41 is thought to undergo dramatic rearrangement from its prefusogenic state. To elucidate this process further, the crystal structure of the SIV gp41 ectodomain (residues 27-149) was determined at 1.47 A resolution and is reported herein. It is the most accurate and complete structure of a retroviral gp41 ectodomain determined to date. The rod-like trimeric structure of SIV gp41 comprises three parallel N-terminal alpha-helices assembled as a coiled coil in the center with three antiparallel C-terminal alpha-helices packed on the outside connected by highly flexible loops. Portions of the loops in all three monomers are crystallographically disordered and could not be accurately modeled. The core of the structure is similar (but not identical) to those of smaller HIV/SIV gp41 segments previously determined by X-ray crystallography with root mean square deviations in main chain atoms of less than 1.0 A. The crystal structure differs more substantially from the reported NMR solution structure of the identical SIV construct. The mechanisms of viral fusion and the inhibition by peptides are discussed in the context of the three-dimensional structure.
人类免疫缺陷病毒(HIV)和猿猴免疫缺陷病毒(SIV)的细胞膜融合是由包膜糖蛋白gp120和gp41介导的。尽管融合过程的确切机制尚不清楚,但人们认为gp41的胞外结构域会从其融合前状态发生显著重排。为了进一步阐明这一过程,本文报道了以1.47 Å分辨率测定的SIV gp41胞外结构域(第27至149位氨基酸残基)的晶体结构。它是迄今为止确定的逆转录病毒gp41胞外结构域最精确和完整的结构。SIV gp41的棒状三聚体结构由三个平行的N端α螺旋组成,它们在中心组装成一个卷曲螺旋,三个反平行的C端α螺旋堆积在外部,由高度灵活的环连接。所有三个单体中环的部分在晶体学上是无序的,无法精确建模。该结构的核心与先前通过X射线晶体学确定的较小HIV/SIV gp41片段的核心相似(但不相同),主链原子的均方根偏差小于1.0 Å。该晶体结构与相同SIV构建体的报道的NMR溶液结构有更大的差异。本文在三维结构的背景下讨论了病毒融合机制和肽的抑制作用。