Mann K, Deutzmann R, Timpl R
Max-Planck-Institut für Biochemie, Martinsried, Federal Republic of Germany.
Eur J Biochem. 1988 Dec 1;178(1):71-80. doi: 10.1111/j.1432-1033.1988.tb14430.x.
Some 12 new nidogen and laminin fragments were purified from elastase, thrombin and trypsin digests and characterized by their sizes (22 kDa to greater than 300 kDa), subunit patterns on electrophoresis, partial amino acid sequences, content of specific epitopes and their binding to laminin or nidogen structures in radioligand assays. This permitted the various fragments to be ordered along the dumbbell-shaped structure of nidogen and to compare them with previously described nidogen fragments arising by endogenous proteolysis. Two nidogen fragments (E-50, E-90; 50 kDa and 90 kDa) remain associated with a large laminin fragment in elastase digests of the complex and could be dissociated with 2 M guanidine.HCl. Recombination studies demonstrated Kd = 10-20 nM for this interaction. Nidogen fragments devoid of binding activity included the tryptic peptide T-40 (40 kDa) corresponding to the rod-like domain and several larger fragments extending more to the N-terminus of nidogen. An N-terminal thrombin fragment of about 50 kDa was also inactive. Together the data show a lack of laminin binding to the N-terminal globule and rod of nidogen and provide indirect evidence that this activity is located within or close to its C-terminal globular domain. Nidogen-binding structures of laminin were obtained as two large fragments (greater than 300 kDa), P1X and E1X. They correspond to the short arm structure of laminin with one (E1X) or two (P1X) arms decreased in size to the inner rod-like segment. Shortening in E1X is mainly due to the B1 chain segment including the central globular domain which was identified as a new laminin fragment E10. Binding of E1X and P1X to nidogen was comparable to that of laminin while much lower activity was found for other laminin fragments. A 10-fold lower binding potential was also observed for the laminin-nidogen complex whose structure can now be defined in more precise molecular terms.
从弹性蛋白酶、凝血酶和胰蛋白酶消化产物中纯化出约12种新的巢蛋白和层粘连蛋白片段,并通过其大小(22 kDa至大于300 kDa)、电泳亚基模式、部分氨基酸序列、特定表位含量以及在放射性配体分析中它们与层粘连蛋白或巢蛋白结构的结合情况进行表征。这使得各种片段能够沿着巢蛋白的哑铃形结构排序,并与先前描述的内源性蛋白水解产生的巢蛋白片段进行比较。在该复合物的弹性蛋白酶消化产物中,两个巢蛋白片段(E-50、E-90;50 kDa和90 kDa)仍与一个大的层粘连蛋白片段结合,并且可以用2 M盐酸胍解离。重组研究表明这种相互作用的解离常数Kd = 10-20 nM。缺乏结合活性的巢蛋白片段包括对应于杆状结构域的胰蛋白酶肽T-40(40 kDa)以及几个延伸至巢蛋白N端更多的较大片段。一个约50 kDa的N端凝血酶片段也无活性。这些数据共同表明层粘连蛋白与巢蛋白的N端球状体和杆状结构缺乏结合,并提供了间接证据表明该活性位于其C端球状结构域内或附近。层粘连蛋白的巢蛋白结合结构以两个大片段(大于300 kDa)P1X和E1X的形式获得。它们对应于层粘连蛋白的短臂结构,其中一个(E1X)或两个(P1X)臂的大小减小至内部杆状片段。E1X中的缩短主要归因于包含中央球状结构域的B1链段,该链段被鉴定为一个新的层粘连蛋白片段E10。E1X和P1X与巢蛋白的结合与层粘连蛋白相当,而其他层粘连蛋白片段的活性则低得多。对于层粘连蛋白 - 巢蛋白复合物,还观察到其结合潜力低10倍,其结构现在可以用更精确的分子术语来定义。