Gallagher T, Alexander P, Bryan P, Gilliland G L
Center for Advanced Research in Biotechnology, University of Maryland Biotechnology Institute, Rockville 20850.
Biochemistry. 1994 Apr 19;33(15):4721-9.
The structure of the 56-residue B1 immunoglobulin-binding domain from streptococcal protein G has been determined in two different crystal forms. The crystal structures were deduced by molecular replacement, based on the structure of the B2 domain (Brookhaven accession code 1PGX). Final R values are 0.174 and 0.198 for orthorhombic and trigonal forms, for diffraction data from 6.0 to 2.07 A and from 6 to 1.92 A, respectively. The orthorhombic crystals have an unusually high packing density for protein crystals, with Vm = 1.66 and a solvent content of 26%. The protein structure is found to be very similar (rms deviation 0.25 A for 56 C alpha's) in the two crystal forms, with an efficiently packed hydrophobic core between a four-stranded beta-sheet and a four-turn alpha-helix. The B1 domain has the same fold and general structure as the B2 domain (rms deviations 0.36 and 0.39 A), despite the six residue differences between them. The crystallographic models differ from NMR-derived models in several local regions, primarily in the loop involving residues 46-51; other significant variations are observed in the helix and in the structure of bound water. The primary crystal contact is the same in both crystal forms, involving both sheet edges to form extended beta-sheets throughout the crystals.
已通过两种不同的晶体形式确定了来自链球菌蛋白G的56个残基的B1免疫球蛋白结合结构域的结构。晶体结构是通过分子置换法推导出来的,以B2结构域的结构(布鲁克海文登录号1PGX)为基础。对于正交晶系和三角晶系形式,分别针对6.0至2.07 Å和6至1.92 Å的衍射数据,最终的R值分别为0.174和0.198。正交晶体对于蛋白质晶体而言具有异常高的堆积密度,Vm = 1.66,溶剂含量为26%。发现两种晶体形式中的蛋白质结构非常相似(56个Cα原子的均方根偏差为0.25 Å),在一个四链β折叠和一个四圈α螺旋之间有一个高效堆积的疏水核心。尽管B1结构域与B2结构域之间存在六个残基差异,但它具有与B2结构域相同的折叠方式和总体结构(均方根偏差为0.36和0.39 Å)。晶体学模型在几个局部区域与核磁共振衍生模型不同,主要在涉及残基46 - 51的环中;在螺旋和结合水的结构中也观察到其他显著差异。两种晶体形式中的主要晶体接触相同,涉及两个片层边缘以在整个晶体中形成延伸的β折叠。