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Progress and challenges in mass spectrometry-based analysis of antibody repertoires
被引:25
|作者:
Snapkov, Igor
[1
,2
]
Chernigovskaya, Maria
[1
,2
]
Sinitcyn, Pavel
[3
]
Khang Le Quy
[1
,2
]
Nyman, Tuula A.
[1
,2
,4
]
Greiff, Victor
[1
,2
]
机构:
[1] Univ Oslo, Dept Immunol, Oslo, Norway
[2] Oslo Univ Hosp, Oslo, Norway
[3] Max Planck Inst Biochem, Computat Syst Biochem, Martinsried, Germany
[4] Univ Oslo, Prote Core Facil PCF, Oslo, Norway
关键词:
MOLECULAR-LEVEL ANALYSIS;
TOP-DOWN;
PEPTIDE IDENTIFICATION;
MONOCLONAL-ANTIBODIES;
SERUM IMMUNOGLOBULINS;
HUMORAL IMMUNITY;
LIGHT-CHAIN;
PROTEOMICS;
CELL;
BINDING;
D O I:
10.1016/j.tibtech.2021.08.006
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Humoral immunity is divided into the cellular B cell and protein-level antibody responses. High-throughput sequencing has advanced our understanding of both these fundamental aspects of B cell immunology as well as aspects pertaining to vaccine and therapeutics biotechnology. Although the protein-level serum and mucosal antibody repertoire make major contributions to humoral protection, the sequence composition and dynamics of antibody repertoires remain underexplored. This limits insight into important immunological and biotechnological parameters such as the number of antigen-specific antibodies, which are for example, relevant for pathogen neutralization, microbiota regulation, severity of autoimmunity, and therapeutic efficacy. High-resolution mass spectrometry (MS) has allowed initial insights into the antibody repertoire. We outline current challenges in MS-based sequence analysis of antibody repertoires and propose strategies for their resolution.
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页码:463 / 481
页数:19
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