Research
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  • Name:Leng Siew Yeap

  • Office Location:Room 903, No. 5 Bldg., West Area, 280 South Chongqing Rd., Shanghai

  • Telephone:86-021-63846590-776726

  • Email:yeaplengsiew@shsmu.edu.cn












Education


2003 U. Msia Sabah B.Sc.



2010 Cambridge University Ph.D.



Career

2003-2005 Genome Institute of Singapore     Research Assistant, Supervisor: Dr Bing Lim
2010-2015 Harvard Medical School, Boston Childrens Hospital, Howard Hughes Medical Institute     Postdoc, Supervisor: Dr Fred Alt
2016-current Shanghai Institute of Immunology,      Principal Investigator

 

Research Interests

Mechanisms of Broadly Neutralizing Antibody Generation

The long term goals of the lab are to elucidate mechanism that generate potent neutralizing antibodies and to establish approaches using such antibodies to fight pathogens and diseases. Specifically, we study the mechanisms of Somatic Hypermutation (SHM), a process whereby point mutations and sometimes insertions and deletions (indels) are introduced in the antibody variable region genes for increase binding affinity of the B cells with antigens. SHM is mediated by a DNA mutator, activation induced cytidine deaminase (AID). While the activities of AID at the immunoglobulin (Ig) genes are important for achieving high-affinity neutralizing antibodies, its off-target activities at non-Ig genes could be disastrous (reviewed in Yeap and Meng, Adv Immunol., 2019). For example, AID targeting at oncogenes such as c-myc and Bcl6 may result in translocation and juxtaposition of the Ig enhancer next to the oncogenes, a hallmark in B cell cancer. Thus, the study of the mechanisms of AID targeting is important in understanding immunity and prevention of cancer.                                                                   

Our lab is particularly interested in studying the mechanisms that generate anti-viral broadly neutralizing antibodies (bnAbs) especially those that are rare and takes a long time to generate such as anti-HIV bnAbs. Such anti-HIV bnAbs have common characteristics such as frequent insertion and deletion in the antibody genes, long CDR3, high frequency of point mutations and are often poly/autoreactive. Our aims are to understand how these special features of the bnAbs are generated during the process of SHM and ultimately apply the knowledge learnt to speed up the process that generate bnAbs. Our long term goal is to establish approaches to efficiently fight diseases and prevent cancer.                                                                                                                                              

                                      

                                                                                          

1.  Huang M.E., Qin Y.N., Shang Y.F., Hao Q., Zhan C.Z., Lian C.Y., Luo S.M., Liu L.D., Zhang S.X., Zhang Y., Wo Y., Li N., Wu S.H., Gui T.T., Wang B.B., Luo Y.F., Cai Y.N., Liu X.J.,Xu Z.Y., Dai P.F., Li S.M., Zhang L., Dong J.C., Wang J., Zheng X.Q., Xu Y.J., Sun Y.H., Wu W., Yeap L.S. *, Meng F.L.*.C-to-G editing generates double-strand breaks causing deletion, transversion and translocation, Nat Cell Biol, 2024, 26(2):294-304.  [Link]

2.  Wang Y.Y., Meng F.L.*,Yeap L.S. *. DNA flexibility can shape the preferential hypermutation of antibody genes, Trends Immunol,2024, S1471-4906(24)00005-X. [Link]

3.  Wang Y.Y., Zhang S.X., Zheng X.Q., Yeap L.S. *, Meng F.L.*. A high-throughput protocol for deamination of long single-stranded DNA and oligo pools containing complex sequences, STAR Protoc, 2023, 4(4):102602. Online ahead of print. [Link]

4.  Wang Y.Y., Zhang S.X., Yang X.R., Hwang J.K., Zhan C.Z., Lian C.Y., Wang C., Gui T.T., Wang B.B., Xie X., Dai P.F., Zhang L., Tian Y., Zhang H.Z., Han C., Cai Y.N., Hao H., Ye X.F., Liu X.J., Liu J.Q., Cao Z.W., Huang S.H., Song J., Pan-Hammarström Q., Zhao Y.F., Alt F.W., Zheng X.Q., Da L.T., Yeap L.S. *, Meng F.L*. Mesoscale dna feature in antibody-coding sequence facilitates somatic hypermutation, Cell, 2023, 186(10): 2193-2207.e19.  [Link]

5.  Hao Q., Zhan C.Z.,  Lian C.Y., Luo S.M., Cao W.Y., Wang B.B, Xie X., Ye X.F., Gui T.T.,  Voena C., Pighi C., Wang Y.Y., Tian Y., Wang X., Dai P.F., Cai Y.N., Liu  X.J., Ouyang S.Q., Sun S.Q., Hu Q.W., Liu J., Ye Y.Q., Zhao J.K., Lu  A., Wang J.Y., Huang C.X., Su B., Meng F.L., Chiarle R.*, Pan-Hammarström Q.*, Yeap L.S.* . DNA  repair mechanisms that promote insertion-deletion events during  immunoglobulin gene diversification, Sci Immunol, 2023,  8(81): eade1167.  [Link]

6.  Gao B., He L.H., Bao Y.J., Chen Y.Y., Lu G.Z., Zhang Y., Xu Y.J., Su B., Xu J.*, Wang Y. *, Yeap L.S.*. Repeated Vaccination of Inactivated SARS-CoV-2 Vaccine Dampens Neutralizing Antibodies Against Omicron Variants in Breakthrough Infection.Cell Res, 2023, 33(3): 258-261.  [Link]  

7.  Lin K., Zhou Y.W., Ai J.W., Wang Y.A., Zhang S.X., Qiu C., Lian C.Y., Gao B., Liu T.T., Wang H.Y., Zhang H.C., Zhang Y., Fu Z.F., Li D., Jiang N., Guo J.X., Wu J., Wang Y.O., Song S.S., Li Q., Yin Y.A., Xia J., Xu Y.J., Yeap L.S., Zheng X.Q., Gu Y., Liu H.Y.*, Zhang W.H.*,  Meng F.L.*. B cell receptor signatures associated with strong and poor SARS-CoV-2 vaccine responses. Emerg Microbes Infect, 2022, 11 (1): 452-464.   [Link]

8.  Feng A.Q, Hao Q* and Yeap L.S.*. Contribution of rare mutational outcomes to broadly neutralizing antibodies. Acta Biochim Biophys Sin (Shanghai), 2022, 54(6): 820-827.  [Link]  

9.  Ye X.F., Ren W.C., Liu D.B., Li X.B., Li W., Wang X.H., Meng F.L., Yeap L.S., Hou Y., Zhu S.D., Casellas, R., Zhang H.L.*, Wu K.*, Pan-Hammarström Q. Genome-wide mutational signatures revealed distinct developmental paths for human B cell lymphomas. J Exp Med, 2021, 218(2):  e20200573.  [Link]

10.  Liu L.D., Lian C.Y., Yeap, L.S.* and Meng F.L.*. The development of neutralizing antibodies against SARS-CoV-2 and their common features. J Mol Cell Biol, 2020, 12(12):  980-986.  [Link]

11.  Tian Y., Lian C.Y., Chen Y.Y., Wei D., Zhang X.X., Ling Y. *, Wang Y. *, Yeap L.S.*. Sensitivity and specificity of SARS-CoV-2 S1 subunit in COVID-19 serology assays. Cell Discov, 2020, 27(6): 75.  [Link]

12.  Liu X.J., Liu TT, Shang Y.F., Dai P.F., Zhang W.B.,  Lee B.J., Huang M., Yang D.P., Wu Q., Liu L.D., Zheng X.Q., Zhou B.O., Dong J.C., Yeap L.S., Hu J.Z., Xiao T.F., Zha S., Casellas R., Liu X.S.* and Meng F.L.*. ERCC6L2 promotes DNA orientation-specific recombination in mammalian cells. Cell Res, 2020, 30(9): 732-744.  [Link]

13.  Yang D.P., Sun Y., Chen J.J., Zhang Y., Fan S.S., Huang M., Xie X., Cai Y.N., Shang Y.F., Gui T.T., Sun L.M., Hu J.Z., Dong J.C., Yeap L.S., Wang X.M., Xiao W. and Meng F.L.*. REV7 is required for processing AID initiated DNA lesions in activated B cells. Nat Commun, 2020, 11(1): 2812.  [Link]

14.  Yeap, L.S.* and Meng F.L.*. Cis- and trans-factors affecting AID targeting and mutagenic outcomes in antibody diversification. Adv Immunol, 2019, 141: 51-103.  [Link]

15.  Liu L.D., Huang M., Dai P., Liu T., Fan S., Cheng X., Zhao Y., Yeap, L.S. and Meng F.L. Intrinsic Nucleotide Preference of Diversifying Base Editors Guides Antibody Ex Vivo Affinity Maturation. Cell Report, 2018, 25: 884-892.  [Link]

16.  Hwang J.K., Wang C., Du Z., Meyers R.M., Kepler T.B., Neuberg D., Kwong P.D., Mascola J.R., Gordon Joyce M., Bonsignori M., Haynes B.F., Yeap L.S.* and Alt F.W.* . Sequence intrinsic somatic mutation mechanisms contribute to affinity maturation of VRC01-class HIV-1 broadly neutralizing antibodies. PNAS, 2017, 1-6.  [Link]

17.  Campagno C., Wang Q., Pighi C., Cheong T.C., Meng F.L., Poggio T., Yeap L.S., Atabay E., Blasco R.B., Langellotto F., Voena C., Kasar S.N., Brown J.R., Sun J., Wu C.J., Gostissa M., Alt F.W and Chiarle R . Phosphatidylinositol 3-kinase δ blockade increases genomic instability in B cells. Nature, 2017, 542(7642): 489-493.  [Link]

18.  Yeap L.S.#, Hwang J.K.#, Du Z., Meyers R.M., Meng F.L., Jakubauskaite, A., Liu M., Mani V., Neuberg D., Kepler T.B., Wang, J.H. and Alt F.W. Sequence-Intrinsic Mechanisms that Target AID Mutational Outcomes on Antibody Genes. Cell, 2015, 163 (5): 1124-37. *co-first authors. Featured in Preview by Cornelis Murre, Cell 163(5):1055-1056.  [Link]

19.  Hwang J.K.#, Alt F.W. and Yeap L.S.#. Related Mechanisms of Antibody Somatic Hypermutation and Class Switch Recombination. Microbiol Spectr, 2015, 3(1):MDNA3-0037-2014. doi:10.1128/microbiolspec.MDNA3-0037-2014.  [Link]

20.  Yeap L.S., Hayashi K. and Surani M.A. ERG-associated protein with SET domain (ESET)-Oct4 interaction regulates pluripotency and represses the trophectoderm lineage. Epigenetics Chromatin, 2009, 2:12.  [Link]

21.  Chew J.L, Loh Y.H., Zhang W., Chen X., Tam W.L., Yeap L.S., Li P., Ang Y.S., Lim B., Robson P. and Ng H.H. Reciprocal transcription regulation of Pou5f1 and Sox2 via the Oct4/Sox2 complex in embryonic stem cells. Mol. Cell. Biol, 2005, 25: 6031-6046.  [Link]



Qian Hao,Ph.D.

Associate Professor

E-mail:haoqian_2016@hotmail.com


103CE

Shengqun Ouyang,M.S

Assistant Engineer

E-mail:shengqunouyang@163.com


8D67

Bo Gao,Ph.D.

Postdoctoral Fellow

E-mail:syaugaobo@163.com


ED6E

Yanyan Wang,Ph.D.

Postdoctoral Fellow

E-mail:wangyanyan2019@sibcb.ac.cn


336DA

Chaoyang Lian

Ph.D. Candidate (Class 2019)

E-mail:liansir@126.com


49C25

Wenyi Cao

Ph.D. Candidate (Class 2020)

E-mail:caowenyi@sjtu.edu.cn


1AC8A

Jinfeng Li

Ph.D. Candidate (Class 2021)

E-mail:dnlijinfeng@163.com


FE59

Shiqi Sun

Ph.D. Candidate (Class 2022)

E-mail:s-black@sjtu.edu.cn



16C4B

Luning Zhang

M.S Candidate (Class 2022)

E-mail:zhangln0223@163.com


120CF

Zi Yin (Graduated)

M.S Candidate (Class 2020)

E-mail:yinzi1030@foxmail.com



29C6B

 

Chuanzong Zhan (Graduated)

Ph.D. Candidate (Class 2018)

E-mail:chuanzongzhan@163.com


106FA

Simin Luo (Graduated)

M.S Candidate (Class 2019)

E-mail:siminluo@126.com





Lab Location:Room 901, No. 5 Bldg., West Area, 280 South Chongqing Rd., Shanghai

Tel:86-021-63846590-776555

 

                 

Copyright 2016. Shanghai Institute of Immunology,Shanghai Jiao Tong University School of Medicine.All Rights Reserved.