Site-Specific Conjugation of Native Antibodies Using Engineered Microbial Transglutaminases

被引:42
|
作者
Dickgiesser, Stephan [1 ]
Rieker, Marcel [1 ,2 ]
Mueller-Pompalla, Dirk [1 ]
Schroeter, Christian [1 ]
Tonillo, Jason [1 ]
Warszawski, Shira [3 ]
Raab-Westphal, Sabine [1 ]
Kuehn, Stefanie [1 ]
Knehans, Tim [1 ]
Koenning, Doreen [1 ]
Dotterweich, Julia [1 ]
Betz, Ulrich A. K. [1 ]
Anderl, Jan [1 ]
Hecht, Stefan [1 ]
Rasche, Nicolas [1 ]
机构
[1] Merck KGaA, D-64293 Darmstadt, Germany
[2] Tech Univ Darmstadt, Clemens Schopf Inst Organ Chem & Biochem, D-64287 Darmstadt, Germany
[3] Merck KGaA, IL-8122004 Yavne, Israel
关键词
THERAPEUTIC INDEX; DRUG; STABILITY; IMPROVES; PHARMACOKINETICS; EXPRESSION; BACTERIAL; EFFICACY; ENABLES; ADCS;
D O I
10.1021/acs.bioconjchem.0c00061
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Site-specific bioconjugation technologies are frequently employed to generate homogeneous antibody-drug conjugates (ADCs) and are generally considered superior to stochastic approaches like lysine coupling. However, most of the technologies developed so far require undesired manipulation of the antibody sequence or its glycan structures. Herein, we report the successful engineering of microbial transglutaminase enabling efficient, site-specific conjugation of drug-linker constructs to position HC-Q295 of native, fully glycosylated IgG-type antibodies. ADCs generated via this approach demonstrate excellent stability in vitro as well as strong efficacy in vitro and in vivo. As it employs different drug-linker structures and several native antibodies, our study additionally proves the broad applicability of this approach.
引用
收藏
页码:1070 / 1076
页数:7
相关论文
共 50 条
  • [1] Site-Specific Conjugation to Native and Engineered Lysines in Human Immunoglobulins by Microbial Transglutaminase
    Spidel, Jared L.
    Vaessen, Benjamin
    Albone, Earl F.
    Cheng, Xin
    Verdi, Arielle
    Kline, J. Bradford
    BIOCONJUGATE CHEMISTRY, 2017, 28 (09) : 2471 - 2484
  • [2] Methods for site-specific drug conjugation to antibodies
    Behrens, Christopher R.
    Liu, Bin
    MABS, 2014, 6 (01) : 46 - 53
  • [3] Site-Specific Antibody Conjugation to Engineered Double Cysteine Residues
    Zhou, Qun
    Kyazike, Josephine
    Boudanova, Ekaterina
    Drzyzga, Michael
    Honey, Denise
    Cost, Robert
    Hou, Lihui
    Duffieux, Francis
    Brun, Marie-Priscille
    Park, Anna
    Qiu, Huawei
    PHARMACEUTICALS, 2021, 14 (07)
  • [4] LASIC: Light Activated Site-Specific Conjugation of Native IgGs
    Hui, James Z.
    Tamsen, Shereen
    Song, Yang
    Tsourkas, Andrew
    BIOCONJUGATE CHEMISTRY, 2015, 26 (08) : 1456 - 1460
  • [5] Affinity-Based Methods for Site-Specific Conjugation of Antibodies
    von Witting, Emma
    Hober, Sophia
    Kanje, Sara
    BIOCONJUGATE CHEMISTRY, 2021, 32 (08) : 1515 - 1524
  • [6] FC SITE-SPECIFIC CONJUGATION OF ALKALINE-PHOSPHATASE TO ANTIBODIES
    HUSAIN, M
    BIENIARZ, C
    FASEB JOURNAL, 1994, 8 (07): : A1358 - A1358
  • [7] Site-specific conjugation on serine → cysteine variant monoclonal antibodies
    Stimmel, JB
    Merrill, BM
    Kuyper, LF
    Moxham, CP
    Hutchins, JT
    Fling, ME
    Kull, FC
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (39) : 30445 - 30450
  • [8] Applications of Galactosyltransferases in the Site-specific Conjugation of Therapeutic Monoclonal Antibodies
    Boeggeman, Elizabeth E.
    Ramakrishnan, Boopathy
    Pasek, Marta
    Waybright, Timothy J.
    Manzoni, Maria R.
    Qasba, Pradman K.
    GLYCOBIOLOGY, 2008, 18 (11) : 998 - 998
  • [9] A NOVEL DERIVATIVE OF THE CHELON DESFERRIOXAMINE FOR SITE-SPECIFIC CONJUGATION TO ANTIBODIES
    POCHON, S
    BUCHEGGER, F
    PELEGRIN, A
    MACH, JP
    OFFORD, RE
    RYSER, JE
    ROSE, K
    INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (06) : 1188 - 1194
  • [10] A Traceless Site-Specific Conjugation on Native Antibodies Enables Efficient One-Step Payload Assembly
    Zeng, Yue
    Shi, Wei
    Dong, Qian
    Li, Wanzhen
    Zhang, Jianxin
    Ren, Xuelian
    Tang, Caihong
    Liu, Bo
    Song, Yuanli
    Wu, Yali
    Diao, Xingxing
    Zhou, Hu
    Huang, He
    Tang, Feng
    Huang, Wei
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2022, 61 (36)